February 13, 2023

FDA Finds Prescription Drug in “100% Natural” Weight Loss Supplement

On February 8, 2023, the FDA warned consumers not to buy or use Alfia 100% Natural Weight Loss Capsules after FDA laboratory analysis confirmed the presence of sibutramine.

January 06, 2015

FDA Warns of Weight Loss Supplement Dangers

On January 5, 2015, the FDA warned consumers that many weight loss products, including supplements, coffees and teas, may promise results they cannot deliver, or contain dangerous hidden drugs.

December 20, 2014

Company Recalls Second Weight Loss Supplement

On December 19, 2014, Bethel Nutritional Consulting, Inc. issued a recall of one lot of weight loss supplement B-Lipo Capsules because they were found to contain Lorcaserin.

August 17, 2021

Weight Loss Supplements Found to Contain Sibutramine Recalled

Two companies (including one Ebay seller) recently recalled weight loss supplements that were found to contain sibutramine.

December 20, 2014

Weight Loss Supplement Recalled

On December 19, 2014, Bethel Nutritional Consulting, Inc. issued a recall of one lot of weight loss supplement SLIM-K Capsules because they were found to contain sibutramine.

October 10, 2014

Weight Loss Supplement Found to Contain Multiple Drugs

On October 10, 2014, the FDA warned consumers not to purchase or use the dietary supplement Japan Hokkaido Slimming Weight Loss Pills because it was found to multiple contain undeclared drugs, including sibutramine, phenolphthalein, benzocaine and diclofenac.

March 19, 2015

Don't Rely on Homeopathic Asthma Products, FDA Warns

On March 19, 2015, the FDA warned consumers who have asthma, or who have a child with asthma, not to rely on homeopathic products that promise to treat asthma or asthma-related symptoms.

July 01, 2003

Direct Marketers of Weight Loss, Impotence, and Arthritis Supplements Charged with Deceptive Claims

On July 1, 2003, the Federal Trade Commission (FTC) announced three enforcement actions against direct marketers of weight-loss products containing ephedra. The two settlements and one complaint, filed in U.S.

November 07, 2005

FTC Stops Bogus Ads for "Bio Trim" and Other Weight-loss Products

On November 7, 2005, the Federal Trade Commission (FTC) announced that under the terms of a consent agreement that it has approved, Tustin, California based Natural Products, LLC, All Natural 4 U, LLC and their owner, Ana M.

January 24, 2017

Weight Loss Supplements Found to Contain Drugs

The FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain undeclared drugs:

December 23, 2016

Weight Loss Supplement Found to Contain Antidepressant

On December 22, 2016, the FDA warned consumers not to buy or use the weight loss supplement Queen Slimming Soft Gel because it was found to contain undeclared fluoxetine and sibutramine.

January 31, 2016

Pink Bikini and Shorts on the Beach Weight Supplements Recalled

On January 28, 2015, Lucy's Weight Loss System issued a voluntary recall of all lots of weight loss supplements Pink Bikini (white capsules, blue capsules and gold capsules) and Shorts on the Beach (blue capsules and gold capsules) because they contain undeclared sibutramine, ...

May 16, 2014

Weight Loss Supplement Found To Contain Drug

On May 16, 2014, the FDA warned consumers not to buy or use weight loss supplement Asset Bold because it was found to contain sibutramine.

December 19, 2020

FDA Finds Unapproved Drugs in Many Weight Loss and Sexual Enhancement Products Sold Online

On December 18, 2020, the FDA warned consumers that certain products promoted for weight loss, body building, sexual enhancement, pain relief, sleep, and other uses because may contain harmful ingredients.

November 01, 2016

Eleven Weight Loss Supplements Contain Undeclared Drugs, FDA Warns

The FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain undeclared drugs:

January 24, 2003

FTC Challenges Weight-loss Claims for Slim Down Solution

The Federal Trade Commission today charged Slim Down Solution, LLC, Maderia Management, Inc., and several related companies and individuals with using false and unsubstantiated claims in the marketing and advertising of "Slim Down Solution" - a purported weight-loss product.

March 19, 2015

Three Weight Loss Supplements Found to Contain Drugs

On March 18, 2015, the FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain undeclared drugs.

May 02, 2015

Drug Found in Two Weight Loss Supplements

The FDA recently warned consumers not to buy or use the following weight loss supplements because they were found to contain sibutramine.

November 24, 2014

Weight Loss Supplement Contains Hidden Drug

On November 24, 2014 the FDA warned consumers not to buy or use weight loss supplement Super Extreme Accelerator because it was found to contain sibutramine.

November 08, 2016

Weight Loss Supplements Contain Hidden Drugs, FDA Warns

The FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain undeclared drugs:

February 04, 2017

Five Weight Loss Supplements Found to Contain Drugs

The FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain undeclared drugs:

March 29, 2016

Weight Loss Supplement Envy BP Contains Undeclared Drug

On March 28, 2016, the FDA warned consumers not to buy or use the weight loss supplement ENVY BP because it was found to contain undeclared sibutramine.

March 20, 2016

FDA Warns of Weight Supplements Containing Undeclared Drugs

On March 17, 2016, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain undeclared drugs:

April 13, 2016

"Super Herbs" Weight Loss Supplement Recalled

On April 11, 2016 Super Herbs issued a recall of all lots of weight loss supplement SUPER HERBS because it was found to contain sibutramine, desmethylsibutramine, and/or phenolphthalein.

December 12, 2015

Pink Bikini Weight Supplement Recalled

On December 9, 2015, Lucy's Weight Loss System issued a voluntary recall of all lots of weight loss supplement Pink Bikini white powder capsules because they were found to contain undeclared diclofenac. 

December 05, 2015

Lipo Escultura Weight Loss Capsules Recalled

On December 3, 2015 Lipo Escultura Corp. (doing business as JAT Productos Naturales Corp.) issued a voluntary recall of weight loss supplement Lipo Escultura capsules because they were found to contain sibutramine and diclofenac.

October 24, 2015

Four Weight Loss Supplements Found To Contain Drugs

On October 23, 2015, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain sibutramine, phenolphthalein and/or sildenfil. Each was identified during an examination of international mail shipments:

October 02, 2015

Drug Found in Two Weight Loss Supplements

On October 1, 2015 the FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain sibutramine:

August 07, 2015

Weight Loss Supplement Found to Contain Drug

On August 6, 2015 the FDA warned consumers not to buy or use the weight loss supplement Achieving Zero because it was found to contain sibutramine. 

July 25, 2015

Weight Supplement Found to Contain Three Drugs

On July 23, 2015 Life & More, L.L.C. issued a voluntary recall of 783 bottles from one lot of Akttive High Performance Fat Burner Gold weight loss capsules because they were found to contain the undeclared drugs sibutramine, desmethylsibutramine, and phenolphthalein.

July 02, 2015

Undeclared Drugs Found in Two Weight Loss Supplements

On July 2, 2015 the FDA warned consumers not to buy or use weight loss supplements listed below because they were found to contain undeclared drugs. Click on the name of each product to read the full warning.

May 19, 2020

FTC Sends Refund Checks to Consumers of Unproven Weight Loss and Sexual Enhancement Supplements

On May 19, 2020, the FTC announced it is mailing 143,636 checks totaling more than $8,500,000 to consumers who purchased deceptively marketed supplements.

January 28, 2020

Weight Supplement Contains Hidden Drug

On January 13, 2020, the FDA issued a warning letter to Wave Miami, LLC because the company's weight loss supplement, Lipro Dietary Capsule was found to contain the prescription medication tadalafil.

March 26, 2021

Nine Banned Stimulants Found in Workout, Weight Loss Supplements

Recent analysis of 17 brands of sports/energy and weight loss supplements sold in the U.S. found nine prohibited stimulants formulated into eight different combinations, and none of these combinations have been studied in people.

August 31, 2004

Two Makers of Weight Loss and Sex Enhancement Supplements Stopped From Making Unsubstantiated Claims

On August 27, 2004, the Federal Trade Commmission (FTC) reported that two Maine-based dietary supplement marketers and their principals have agreed to settle FTC charges that they made deceptive advertising claims about their dietary supplement products, in violation of federal law.

June 19, 2013

Weight Loss Supplements Found To Contain Undeclared Drugs, FDA Warns

On June 17, 2013, the FDA advised consumers not to purchase or use the weight loss supplements listed because they were found to contain one or both of the undeclared drugs sibutramine and phenolphthalein.

November 05, 2014

Slimming Coffee Found to Contain Drug

On November 4, 2014, the FDA warned consumers not to purchase or use the dietary supplement V26 Slimming Coffee because it was found to contain sibutramine.

October 10, 2014

FDA Warns Consumers of Weight Loss Supplement Containing Undeclared Drugs

On October 10, 2014, the FDA warned consumers not to purchase or use the dietary supplement Sit and Slim II because it was found to contain sibutramine and phenolphthalein.

September 13, 2014

Three Weight Loss Supplements Found to Contain Drugs

On September 12, 2014, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain drugs.

February 26, 2015

Weight Loss Supplement Found to Contain Multiple Drugs

On February 25, 2015, the FDA warned consumers not to buy or use weight loss supplement Lean Body Extreme because it was found to contain sibutramine, desmethyl sibutramine, phenolphthalein, and sildenafil.

February 10, 2015

Five Weight Loss Supplements Recalled

On January 9, 2015, Detox Transforms Health and Nutrition issued a voluntary recall of five weight loss supplements because they were found to contain undeclared drugs:

February 03, 2015

Weight Loss Supplement Contains Hidden Drug

On February 3, 2015, the FDA warned consumers not to buy or use weight loss supplement Yanhee Slim because it was found to contain lorcaserin.

March 13, 2015

Weight Loss Supplement Contains Prescription Anti-Depressant, Other Drugs

On March 3, 2015, the FDA warned consumers not to buy or use weight loss supplement Natural Max Slimming because it was found to contain fluoxetine, sildenafil and sibutramine.

March 26, 2015

Green Algae Weight Loss Supplement Contains Hidden Drug

On March 26, 2015, the FDA warned consumers not to buy or use weight loss supplement Green Algae Combination (Crane Beauty) because it was found to contain lorcaserin.

March 13, 2015

Weight Supplement Containing Drugs Recalled

On March 10, 2015, UltraZx, Labs, L.L.C, issued a voluntary recall of all lots of weight loss supplement UltraZx because it was found to contain undeclared sibutramine and phenolphthalein.

March 06, 2015

FDA Warns Consumers Not to Buy or Use Weight Loss Supplement Containing Hidden Drug

On March 5, 2015, the FDA warned consumers not to buy or use weight loss supplement L-Carnitine Sob Strengthening Version Slimming Miracle Capsule because it was found to contain sibutramine.

March 03, 2015

FDA Warns Consumers Not to Buy or Use Weight Loss Supplement Containing Drug

On February 28, 2015, the FDA warned consumers not to buy or use weight loss supplement Oxy ELITE Pro Super Thermogenic (USPLabs) because it was found to contain fluoxetine.

March 02, 2015

Weight Loss Supplement Found to Contain Drug

On February 28, 2015, the FDA warned consumers not to buy or use weight loss supplement Nine Slim because it was found to contain phenolphthalein.

May 01, 2014

Weight Loss Supplement Recalled

On April 29, 2014, dietary supplement distributor Bacai Inc. issued a voluntary recall of one lot of weight loss supplement LiteFit USA because it was found to contain sibutramine.

April 18, 2014

Weight Loss Supplement Recalled

On April 9, 2014, Nature's Universe issued a voluntary recall of all lots of Thinogenics weight loss capsules sold prior to February 6, 2014 because they were found to contain sibutramine.

June 11, 2014

FDA Warns Consumers Not to Buy or Use Weight Loss Supplement

On June 10, 2014, the FDA warned consumers not to buy or use weight loss supplement La Jiao Shou Shen because it was found to contain sibutramine and phenolphthalein.

June 05, 2014

FDA Warns Consumers Not to Buy Use Weight Loss Supplement Containing Hidden Drugs

On June 5, 2014, the FDA warned consumers not to buy or use weight loss supplement B-Perfect because it was found to contain sibutramine and phenolphthalein.

March 27, 2014

Three Weight Loss Supplements Containing Drugs Recalled

On March 25, 2014, New Life Nutritional Center issued a voluntary recall of all lots of Super Fat Burner capsules, Maxi Gold capsules and Esmeralda softgels because they were found to contain sibutramine, phenolphthalein or a combination of both drugs.

October 10, 2013

Six Weight Loss Supplements Found to Contain Drugs

On October 10, 2013, the FDA advised consumers not to purchase or use the six weight loss supplements listed below because they were found to contain one or both of the undeclared drugs sibutramine and phenolphthalein.

August 08, 2013

Weight Loss Supplement Containing Undeclared Drug Recalled

On August 3, 2013, CTV Best Group issued a voluntary recall of all lots of weight loss supplement BEST SLIM because it was found to contain sibutramine.

August 06, 2013

Weight Loss Supplement Recall Expanded

On August 5, 2013, Bethel Nutritional Consulting, Inc., issued a voluntary recall of herbal weight loss supplements Quick Thin and Bethel Advance because they were found to contain sibutramine and phenolphthalein.

September 09, 2015

Weight Supplement Found to Contain Drug

On September 3, 2015 the FDA warned consumers not to buy or use the weight loss supplement Meizi Super Power Fruits Herbal Slimming Formula because it was found to contain sibutramine.

November 21, 2015

Ultimate Herbal Slimcaps Recalled

On November 19, 2015 Fit Firm and Fabulous issued a voluntary recall certain lots of weight loss supplement Ultimate Herbal Slimcap capsules because they were found to contain sibutramine.

November 10, 2015

"Natureal" Weight Supplement Recalled

On November 9, 2015 Inaffit, LLC issued a voluntary recall of all lots of weight loss supplement Natureal because it was found to contain undeclared sibutramine.

December 23, 2015

"Bee Extremely Amazed" Recalls Weight Supplements

On December 22, 2015, Bee Extremely Amazed LLC issued a voluntary recall of all lots of the following weight loss supplements, which were found to contain sibutramine and phenolphthalein: 

November 11, 2016

FDA Warns Consumers Not to Use Weight Loss Supplement

On November 9, 2016, the FDA warned consumers not to buy or use the weight loss supplement Supreme Slim 5.7 because it was found to contain sildenafil and phenolphthalein.

April 16, 2014

Weight Loss Supplements Found To Contain Prescription Antidepressant and Other Drugs

On March 7, 2014, the FDA issued a warning letter to Deseo Rebajar Inc. because the company's following weight loss products were found to contain drugs:

September 15, 2005

Weight Loss Pill Marketer in Settlement with New Jersey Attorney General

On August 16, 2005, New Jersey Attorney General Peter C. Harvey and Consumer Affairs Director, Kimberly Ricketts, announced that Goen Technologies Corp.

April 11, 2014

Two Weight Loss Supplements Found to Contain Drug

On April 10, 2014, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain sibutramine.

April 03, 2014

Weight Loss Supplement Containing Drugs Recalled

On April 2, 2014, the FDA warned consumers not to buy or use weight loss supplement New You because it was found to contain sibutramine and phenolphthalein.

June 18, 2014

Two Weight Loss Supplements Found to Contain Drugs

On June 17, 2014, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain drugs.

May 06, 2014

Two Weight Loss Supplements Found To Contain Drug

On May 5, 2014, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain sibutramine.

March 27, 2014

Bee Pollen and Weight Loss Supplements Recalled

On March 26, 2014, Pure Edge Nutrition, LLC issued a voluntary recall of Bella Vi Insane Bee Pollen Capsules, Bella Vi BTrim Ultimate Boost, Bella Vi BTrim Max, Bella Vi Extreme Accelerator, Bella Vi Insane Amp'd, and two lots of Bella Vi Amp'd Up because they were found to contain sibutramine, ...

March 19, 2014

Weight Loss "Coffee" Found to Contain Drug

On March 19, 2014, the FDA warned consumers not to buy or use Vitaccino Coffee because it contains sibutramine.

February 28, 2014

Weight Loss Supplement Contains Undeclared Drug

On February 18, 2014, Health Canada warned consumers not to use weight loss supplement LV Shou Reduces Fat because it contains sibutramine.

January 09, 2014

Four Companies Settle FTC Charges of Deceptive Weight Loss Claims

On January 7, 2014, the Federal Trade Commission (FTC) announced that marketers for four weight loss products have agreed to settlements over charges of deceptive weight loss claims.

August 20, 2013

Weight Loss Supplement Formulas For Men and Women Recalled Due To Undeclared Drugs

On August 16, 2013, Herbal Give Care LLC issued a voluntary recall of all lots of weight loss dietary supplements Esbelder man, Esbelder fem and Esbelder siloutte because they were found to contain the undeclared drugs sibutramine, N-desmethylsibutramine, and N-di-desmethylsibutramine.

June 30, 2013

Weight Loss Supplements Recalled Due To Undeclared Drug

On May 21, 2013, the Dolphin Intertrade Corp. issued a voluntary recall of one lot of weight loss supplement JaDera and all lots of weight loss supplement Xiyouji Qingzhi, which were found to contain the undeclared drug sibutramine.

November 30, 2013

"Diuretic" Weight Loss Supplement Recalled

On November 29, 2013, IQ Formulations issued a recall of all lots of diuretic weight loss supplement HYDRAVAX because one lot of the supplement was found to contain an undeclared prescription diuretic drug.

March 03, 2015

Weight Supplement Contains Hidden Drug

On March 2, 2015, the FDA warned consumers not to buy or use weight loss supplement Elimulating Weight & Toxin Keeping Beauty because it was found to contain sibutramine.

May 13, 2015

Amberen Weight Loss Claims Not Supported by Evidence, Says FTC

On May 12, 2015, the FTC announced it filed a complaint to stop Lunada Biomedical Inc. from advertising that its product Amberen is clinically proven to cause substantial weight loss in women over 40.

June 06, 2015

Weight Supplement Recalled

On June 3, 2015 SmartLipo365 issued a voluntary recall of 122 lots of Smart Lipo because they were found to contain the undeclared drugs sibutramine, desmethylsibutramine, and phenolphthalein.

November 26, 2014

Weight Loss Supplement Found to Contain Hidden Drug

On November 25, 2014, the FDA warned consumers not to buy or use weight loss supplement Slim Vie because it was found to contain sibutramine.

September 13, 2014

Marketer Banned From Selling Weight Loss Products

In order to settle FTC charges of deceptive weight loss claims, John Matthew Dwyer III, the co-founder of HealthyLife Sciences, LLC, has agreed to no longer manufacture or market weight loss supplements.

February 06, 2016

Marketers of Weight Supplements AF Plus and Final Trim Violated Consumer Protection Laws, Says FTC

On January 19, 2016, the Federal Trade Commission (FTC) and State of Maine's Office of the Attorney General charged marketers of weight loss supplements AF Plus and Final Trim with violating consumer protection laws.

December 01, 2015

Weight Supplements Found to Contain Antidepressant and Other Prescription Drugs

On November 19, 2015, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain prescription drugs. Each was identified during an examination of international mail shipments:

October 16, 2018

Weight Loss Supplement Containing Hidden Drug Recalled

On October 15, 2018, Fat Burners Zone issued a recall of one lot of its Zero Xtreme weight loss supplement because it was found to contain sibutramine.

January 29, 2019

Prescription Drugs Found in Four Weight Loss Supplements

On January 28, 2019, the FDA the FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain sibutramine and/or phenolphthalein:

January 22, 2019

Weight Loss Supplement Tainted With Drug

On January 10, 2019, the FDA warned consumers not to use the weight loss supplement Slimina, because it was found to contain sibutramine.

September 14, 2023

Toxic Herb Found In Weight Supplements

On September 8, 2023, the FDA warned consumers that Nut Diet Max and Todorganic Natural Products brand supplements and seed products labeled as containing "Nuez de la India" (Aleurites moluccana) seeds actually contain yellow oleander (Thevetia ...

June 19, 2018

FDA Warns Seller of Weight Control Patches

On June 6, 2018, the FDA issued a warning letter to Health Management Group, Inc.

July 27, 2021

"Miss Slim" Capsules Recalled

On July 20, 2021, HIS issued a recall of all lots and presentations of Miss Slim capsules because FDA analysis found them to contain sibutramine.

December 09, 2021

Florida Man Convicted for Distributing Steroids Labeled as Dietary Supplements

On December 9, 2021, 37-year-old Florida resident James Boccuzzi was convicted of one count of conspiracy to defraud the U.S. Food and Drug Administration (FDA) and one count of conspiracy to distribute controlled substances.

July 10, 2014

Five Weight Loss Supplements Found to Contain Undeclared Drugs

On July 8, 2014, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain undeclared sibutramine and/or phenolphthalein.

December 20, 2013

Five Weight Loss Supplements Found to Contain Undeclared Drug

On December 19, 2013, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain undeclared sibutramine.

November 21, 2013

Weight Loss Supplement Recalled

On November 14, 2013, Deseo Rebajar Inc. issued a recall of one lot of weight loss supplement Adipotrim XT because it was found to contain undeclared fluoxetine.

July 23, 2013

Weight Loss Supplements Containing Undeclared Drugs Recalled

On July 19, 2013, Herbal Give Care LLC issued a voluntary recall of all lots of weight loss supplements Esbelin siloutte te and Esbelin siloutte Herbal Blend with L-Carnitine because they were found to contain undeclared sibutramine, N-desmethylsibutramine, and N-di-desmethylsibutramine.

October 09, 2014

New Synthetic Stimulant Found in Supplements

A synthetic stimulant never before studied in humans, 1,3-dimethylbutylamine (DMBA), was found in a dozen supplements sold by U.S. distributors in dosages from 13 to 20 mg per serving (Cohen, Drug Test Analys 2014).

October 22, 2014

Supplements Recalled Years Ago Remain on the Market, Still Contain Hidden Drugs

On October 21, 2014, a report in the Journal of the American Medical Association (JAMA) revealed that almost 10% of the supplements that have been recalled over the past few years are still on the market - and many still contain the hidden drugs which prompted their initial recall.

November 25, 2014

FDA Warns Consumers Not to Buy or Use Weight Loss Supplement

On November 24, 2014, the FDA warned consumers not to buy or use weight loss supplement Bee Slim because it was found to contain sibutramine.

December 12, 2014

Marketers of HCG Settle FTC Charges of Deceptive Weight Loss Claims

Marketers of HCG Platinum drops have agreed to pay $1 million to settle Federal Trade Commission (FTC) charges that claims the drops could cause rapid and substantial weight loss were deceptive and not supported by scientific evidence.

July 03, 2016

Weight Loss Supplement Recalled

On June 1, 2016, Dream Body Weight Loss issued a recall of all lots of the following weight loss supplements listed because they were found to contain undeclared sibutramine:

• Dream Body Extreme Gold 800 mg 30 gold capsules

April 01, 2017

Weight Loss Supplement Containing Undeclared Drug Recalled

On March 28, 2017, Envy Me issued a recall of weight loss supplement LaBri's Body Health Atomic because it was found to contain undeclared sibutramine. Sibutramine, the active ingredient in the obesity drug Meridia, was removed from the U.S.

May 01, 2023

TruVision Recalls Products Due to Presence of Potentially Dangerous Ingredients

On April 27, 2023, TruVision Health issued a recall of various dietary supplement products because they contain hordenine and/or octodrine/DMHA, compounds that the FDA considers to be “possibly unsafe” and which are not permitted to be sold as dietary supplements.

February 21, 2015

FTC Mails Refund Checks to Consumers Who Purchased Weight Loss Pills

As part of a $500,000 settlement over "outrageous" weight-loss claims made by a supplement company called the "Freedom Center Against Obesity," the FTC is mailing 11,585 refund checks this week to consumers who purchased the company's Double Shot diet pills.

December 10, 2002

Company Ordered to Cease Deceptive Marketing of Weight Loss Product

A U.S. District Court in Texas has ordered Mark Nutritionals, maker of Body Solutions Evening Weight Loss Formula, to stop making certain claims with regard to the product. The order is in response to a complaint by the Federal Trade Commission (FTC) accusing the company of false advertising.

May 11, 2006

Weight-Loss Marketers Pay $3 Million for Deceptive Advertising

On May 11, the Federal Trade Commission (FTC) announced that sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle charges that their deceptive claims violated federal law.

June 21, 2005

Marketers of “Himalayan Diet Breakthrough” Settle FTC Charges of Deceptive Advertising

On June 20, the Federal Trade Commission (FTC) announced that AVS Marketing, Inc., and its president, William R. Heid, have agreed to pay $400,000 in consumer redress to settle FTC charges that they deceptively marketed a purported weight-loss pill called “Himalayan Diet Breakthrough.

November 21, 2014

Weight Loss Supplements Recalled

On November 19, 2014, REFA Enterprises, LLC issued a voluntary recall of one lot each of Forever Beautiful Bee Pollen and Forever Beautiful Infinity because they were found to contain sibutramine or a combination of sibutramine and phenolphthalein.

May 09, 2015

Marketers Charged with Using Stolen Email Accounts to Promote Weight Loss Supplements Temporarily Shut Down

On May 4, 2015, the FTC announced it has obtained a court order to temporarily halt the operations of weight loss marketers Sale Slash, charging that the company used affiliate marketers to send illegal spam emails and post banner ads online that led consumers to fake news sites.

June 27, 2013

Two Weight Loss Supplements Found To Contain Undeclared Drugs

On June 27, 2013, the FDA warned consumers not to use or buy two dietary supplements for weight loss which were found to contain the undeclared sibutramine and/or phenolphthalein.

November 21, 2013

FDA Warns of Five More Weight Loss Supplements Containing Undeclared Drugs

On November 21, 2013, the FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain one or both of the undeclared drugs sibutramine and phenolphthalein:

November 20, 2013

Weight Loss Supplement Found to Contain Drugs

On November 19, 2013, the FDA warned consumers not to buy or use weight loss supplement Slim Max because it was found to contain sibutramine and phenolphthalein.

November 12, 2013

Weight Loss Supplement Found To Contain Drugs

On November 8, 2013, Health Canada warned consumers of a number of weight loss products that have been found to contain sibutramine or phenolphthalein, including Paiyouji Natural Slimming Capsules, which may be available for purchase to U.S. consumers through online retailers.

November 06, 2013

Weight Loss Supplement Found to Contain Drugs

On November 5, 2013, the FDA advised consumers not to purchase or use the weight loss supplement Goodliness Fat-Reducing capsules, which were sold on various websites, because they were found to contain sibutramine and phenolphthalein.

December 24, 2013

FDA Warns Consumers Not to Buy or Use Weight Loss Supplement

On December 19, 2013, the FDA warned consumers not to buy or use weight loss supplement Dr. Ming's Chinese Capsule because it was found to contain sibutramine and phenolphthalein.

February 17, 2014

Weight Loss Supplement Recall Expanded to Include Additional Products

On February 4, 2014, MyNicKnaxs, LLC, which first issued a recall of Reduce Weight Fruta Planta, issued a recall of nine additional weight loss supplements: Magic Slim, Fruta Bio, SlimEasy, Super Fat Burning Bomb, Slim Xtreme, Meizi Evolution, Meizitang Strong Version Botanical Slimming, ...

May 15, 2014

FDA Warns Consumers Not To Buy Or Use Weight Loss Supplement

On May 12, 2014, the FDA warned consumers not to buy or use weight loss supplement Asset Bee Pollen because it was found to contain sibutramine.

August 20, 2016

Smart Lipo Weight Loss Supplement Found to Contain Undeclared Drugs

On June 16, 2016, the FDA issued a warning letter to Centro Naturista because the company's weight loss supplement, Smart Lipo, was found to contain undeclared sibutramine and phenolphthalein.

May 02, 2016

Weight Loss Supplements Containing Hidden Drugs Recalled

On April 29, 2016 Making It A Lifestyle, L.L.C. issued a recall of all lots of weight loss supplements 3rd Degree, Black Gold X Advanced and Black Label X because they were found to contain undeclared sibutramine and sildenafil.

February 05, 2016

Garcinia, Green Coffee Marketers Pay $43 Million to Settle Charges of False Weight Loss Claims

Sale Slash, LLC, has agreed to pay more than $43 million to settle FTC charges it used unsubstantiated claims and fake celebrity endorsements to promote its Premium Green Coffee, Pure Garcinia Cambogia, Premium White Kidney Bean Extract, Pure Forskolin Extract, and Pure Caralluma Fimbriata Extract ...

December 19, 2015

Don't Get Stung by Bee Pollen

On December 18, 2015, the FDA warned consumers not to buy or use the following supplments promoted for weight loss because they were found to contain sibutramine and phenolphthalein:

April 14, 2020

Teami Tea Settles Charges of Unproven Claims and Deceptive Celebrity Endorsements

On March 6, 2020, the FTC announced that Teami, LLC, a marketer of tea and skin care products, agreed to settle charges that it was selling products with unproven claims and misleading celebrity endorsements.

October 24, 2003

Court Closes the Doors on Company That Sold Weight Loss Supplement

On October 24, 2003, the Federal Trade Commission (FTC)announced that Mark Nutritionals, Inc. and Edward D’Alessandro, Jr. have agreed to settle federal charges that they used false and unsubstantiated claims to sell their weight-loss product.

July 26, 2017

Weight Loss Supplements Containing Undeclared Drug Recalled

On July 25, 2017, EZ Weight Loss TX recalled their supplements La Bri's Body Health Atomic and Xplode capsules after FDA analysis found the products to be tainted with sibutramine.

July 30, 2003

Maker of Weight-Loss and Cellulite Treatment Ordered to Stop False Claims and Pay Consumer Redress

On July 30, 2003 the Federal Trade Commission (FTC) reported that a Canadian-based company operating in the United States under the name “Bio Lab,” and its president, Jean-Francois Brochu, have agreed to settle FTC charges that they deceived consumers through false and unsubstantiated advertising ...

April 03, 2012

“Japan Rapid Weight Loss Diet Pills Green” Contains Hidden Drug Ingredient

April 3, 2012: The Food and Drug Administration (FDA) is advising consumers not to purchase or use "Japan Rapid Weight Loss Diet Pills Green," a product for weight loss sold on various websites, such as www.amazon.com, and distributed by Xiushentang.

December 08, 2011

HCG Diet Products Don't Work and Are Illegal Says FDA

On December 6, 2011, the U.S. FDA warned consumers to avoid homeopathic HCG weight-loss diet products because they don't work, often make unsupported claims, and are illegal for sale. In addition, some of these products direct user to follow a potentially dangerous diet.

January 04, 2007

Sellers of Popular Weight Loss Supplements Pay $25 Million Over FTC Allegations of Deceptive Advertising

On January 4, 2007, the Federal Trade Commission (FTC) announced that it had filed complaints in four separate cases alleging that weight-loss and weight-control claims were not supported by competent and reliable scientific evidence.

February 22, 2012

"Japan Weight Loss Blue" Pills Dangerous According to FDA

On February 18, 2012, the U.S. Food and Drug Administration (FDA) advised consumers not to purchase or use “Japan Weight Loss Blue,” a product for weight loss sold on various websites, including www.vitaminbestbuy.com.

June 14, 2013

Weight Loss Supplement Found To Contain Undeclared Drug

On June 6, 2013, the FDA warned consumers that weight loss dietary supplement XIYOUJI QINGZHI CAPSULE was found to contain undeclared simbutrimine.

June 12, 2013

Weight Loss Supplement Recalled Due To Undeclared Drugs

On June 11, 2013, Bethel Nutritional Consulting, Inc. issued a voluntary recall of one lot of Bethel 30 herbal weight loss supplement because it was found to contain undeclared sibutramine and phenolphthalein.

February 14, 2014

Weight Loss Supplement Containing Drug Recalled

On February 4, 2014, MyNicKnaxs, LLC. issued a recall of weight loss supplement Reduce Weight Fruta Planta because it was found to contain phenolphthalein.

January 30, 2014

Four Weight Loss Supplements Found To Contain Drugs

On January 28, 2014, the FDA warned consumers not to buy or use the four weight loss supplements listed below because they were found to contain sibutramine or phenolphthalein.

January 23, 2014

"Slimming" Supplements Found to Contain Drugs

On January 21, 2014, the FDA advised consumers not to buy or use weight loss supplements Dream Body Slimming Capsule and Magic Slim because they were found to contain sibutramine and/or phenolphthalein.

November 07, 2013

FDA Warns Consumers of Weight Loss Supplement Containing Multiple Drugs

On November 7, 2013, the FDA warned consumers not to buy or use Jimpness Beauty Fat Loss Capsules because they were found to contain sibutramine, phenolphthalein, and sildenafil.

October 21, 2014

Seller of Weight Loss Supplements Warned for Manufacturing Violations and Drug Claims

On October 7, 2014, the FDA issued a warning letter to YoungYou International, Inc.

September 09, 2014

Maker of Popular Green Coffee Bean Extract Settles FTC Charges of Unsupported Weight Loss Claims

Applied Food Sciences, Inc., maker of green coffee bean extract GCA, has agreed to pay $3.5 million to settle FTC charges that weight loss claims made about the extract were not supported by scientific evidence.

December 19, 2015

"Thirty Plus" Contains Hidden Drug

On December 18, 2015, the FDA warned consumers not to buy or use the weight loss supplement Thirty Plus because it was found to contain sibutramine.

December 19, 2015

Drugs Found in Jenesis Weight Supplement

On December 18, 2015, the FDA warned consumers not to buy or use the weight loss supplement Jenesis because it was found to contain sibutramine and phenolphthalein.

May 07, 2016

Weight Loss Supplement Contains Hidden Drug, FDA Warns

On May 6, 2016 the FDA warned consumers not to buy or use weight loss supplement Step 2 because it was found to contain undeclared sibutramine.

June 07, 2016

Step 2 Weight Loss Supplement Recalled

On June 7, 2016, The Body Shot Bar issued a recall of all lots of weight loss supplement Step 2 60 gold capsule (350 mg per) capsules which were distributed between March 1 through May 6 2016 because they were found to contain undeclared sibutramine.

March 16, 2018

FTC Sends Refund Checks to Consumers of Unproven Weight-Loss Products

On March 15, 2018, the FTC announced it is mailing 18,301 checks totaling more than $437,000 to consumers who purchased weight-loss products from Colby Fox, Christopher Reinhold, and their companies, Tachht, Inc. and Teqqi, LLC.

February 27, 2018

Weight Loss Supplement Containing Undeclared Drug Recalled

On February 27, 2018, Bella All Natural recalled their "Diet Capsules" because they contain sibutramine. 

June 20, 2019

Weight Loss, Muscle & Energy Supplements Linked to Adverse Events in Children and Young Adults

Consumption of dietary supplements sold for weight loss, muscle building, and energy are associated with an increased risk for severe medical events in children and young adults compared to the consumption of vitamins, according to a recent study published in the Journal of the Adolescent ...

March 06, 2019

GoLean Detox Recalled

On February 25, 2019, GoLean Detox USA issued a recall of all lots of GoLean DETOX capsules within expiry because they were found to contain sibutramine and phenolphthalein.

May 11, 2022

FDA Warns 10 Companies for Selling Workout Supplements With Dangerous Ingredients

On May 4, 2022, the FDA issued warning letters to 10 companies for selling products promoted for muscle building, fat burning and other uses that contain potentially dangerous ingredients not permitted in dietary supplements, including hordenine, higenamine, 5-alpha-hydroxy-laxogenin, and CBD.

April 29, 2024

Longreen Reishi and Xlim Express Coffee Recalled Due to Undeclared Allergens

On April 18, 2024, BF Suma Pharmaceuticals, Inc.

December 19, 2024

Toxic Herb Found in More Weight Loss Supplements

On December 13, 2024, Motivate Me Ashley, LLC recalled the following VidaSlim brand products: VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsules), VidaSlim 7-day Sample Size (Original Root, Root Plus, and ...

December 12, 2014

FTC Mails Refund Checks to Consumers Who Purchased Sensa

As part of a $26,023,329 settlement over false weight-loss claims made by marketers of Sensa, the FTC is mailing 477,083 refund checks this week to consumers who purchased Sensa "sprinkles."

April 21, 2011

FTC Targets Fake News Sites Making Deceptive Acai Claims

On April 19, 2011, the Federal Trade Commission (FTC) requested federal courts to temporarily halt the allegedly deceptive tactics of 10 operations using fake news websites to market acai berry weight-loss products.

January 09, 2009

FDA Expands Warning to Consumers About Tainted Weight Loss Pills

On January 8, 2009, the U.S. FDA expanded its nationwide alert to consumers about tainted weight loss pills that contain undeclared, active pharmaceutical ingredients. On December 22, 2008, FDA warned consumers not to purchase or consume 28 different products marketed for weight loss.

July 23, 2009

Weight Loss Supplements Found to Contain Prescription Drug

On July 15, 2009, the U.S. FDA announced that Young You Corporation was recalling four weight loss supplements that contain an undeclared drug ingredient.

April 04, 2013

FDA Warns Consumers Of Weight Loss Supplement Containing Undeclared Drug

On April 4, 2013, the FDA warned consumers not to purchase or use the dietary supplement MAXILOSS Weight Advanced Blue because it was found to contain sibutramine.

February 25, 2013

Weight Loss Supplement Recalled Due To Undeclared Drug

On February 21, 2013, Olaax Corp. issued a voluntary, nationwide recall of the company's weight loss supplement MAXILOSS Weight Advanced softgels because they were found to contain undeclared Sibutramine.

January 27, 2015

Green Coffee Bean Supplement Marketer Settles FTC Charges of Deceptive Claims

On January 26, 2015, the FTC announced that Pure Health LLC, Genesis Today, and owner of both companies, Lindsey Duncan, will pay $9 million to settle charges of deceptive weight loss claims made about the companies' green coffee bean extract products.

September 02, 2014

Recall of Weight Loss Supplement Expanded

On August 27, 2014, Regeneca Worldwide expanded its previous recall of two lots of appetite control supplement RegenESlim to include two more lots because FDA tests found them to contain DMAA (1,3-dimethylamylamine).

December 26, 2013

Weight Loss Supplement Recalled

On December 23, 2013, Deseo Rebajar Inc. issued a voluntary recall of one lot of Burn 7 Capsules because they were found to contain sibutramine.

April 02, 2016

Propell Platinum Contains Undeclared Drugs

On March 29, 2016, the FDA warned consumers not to buy or use the weight loss supplement Propell Platinum because it was found to contain undeclared sibutramine and phenolphthalein.

January 19, 2023

Male Sexual Enhancement Supplement Adam’s Secret Found to Contain Prescription Medication

On January 10, 2023, the FDA issued a warning letter to HIS Enterprise Inc dba Adam’s Secret USA, LLC after laboratory analysis found Adam’s Secret Extra Strength 3000 Platinum, Adam’s Secret Extra Strength Blue, Adam’s Secret Extra Strength Purple, Adam's Secret ...

November 29, 2012

Sensa Settles Second False Advertising Lawsuit

On November 27, 2012, Sensa Products LLC, maker of the Sensa Weight Loss System, announced it agreed to settle a false advertising lawsuit filed by the Nutritional Supplemental Task Force in California, without an admission of guilt.

November 02, 2009

FTC Charges Marketers with Baseless Weight-Loss Claims

On November 2, 2009 the U.S. Justice Department, at the Federal Trade Commission’s request, filed suit today in federal court in a case affecting consumers nationwide.

June 21, 2005

FTC Settles Claims with Marketers of FiberThin and Propolene

On June 20, 2005, the Federal Trade Commission (FTC) announced that the marketers of the dietary supplements FiberThin and Propolene have settled FTC charges that their misleading weight-loss claims violated federal laws.

June 17, 2004

FTC Challenges Deceptive Weight Loss Claims for Supplement Targeted at Hispanics

On June 17, 2004, the Federal Trade Commission (FTC) announced a new law enforcement action challenging false advertising for the 1-2-3 Diet Kit, a purported weight loss product.

January 18, 2005

Sellers of “Fat Trapper Plus” and “Exercise in a Bottle” Banned from Advertising Weight-Loss Products

On January 18, 2005, the Federal Trade Commission (FTC)announced that Enforma Natural Products, Inc.

September 10, 2021

FDA Warns Ten Sellers of "Diabetes" Supplements

On September 7, 2021, the FDA issued warning letters to 10 supplement companies that made drug claims by promoting products to treat diabetes and/or lower blood sugar. Five of the products were sold on Amazon as well as on company websites. The products were promoted with statements such as

June 16, 2004

Ads for Various Diet Pills and Topical Gels Don’t Cut the Fat, Says the FTC

On June 16, 2004, The Federal Trade Commission (FTC)charged a Utah-based company, five related corporations, and three individuals operating as a common enterprise with making numerous false and unsubstantiated claims for weight-loss and fat-loss gels and supplements.

June 08, 2018

NutriMost Weight-Loss System Consumers Can Submit Claim for Refund

On May 17, 2018, the FTC announced consumers who purchased the NutriMost Ultimate Fat Loss System in the Pittsburgh, Pennsylvania, area between October 1, 2012, and August 9, 2016 can now submit a claim for a refund as part of settle agreement. The refund claim form can be found here.

August 17, 2022

Seller of Moringa Tea and Other Herbal Products Warned for Drug Claims, Manufacturing Violations

On July 29, 2022, the FDA issued a warning letter to Deggeh Foods, Inc.

August 25, 2022

White Mulberry Leaf Caused Death of Congressman's Wife, Coroner Reports

The death of Lori McClintock, 61-year-old wife of California congressman Tom McClintock, was caused by dehydration from gastroenteritis caused by “adverse effects of white mulberry leaf ingestion,” according to a coroner's report recently obtained by Kaiser Health News.

April 28, 2017

Marketers of Weight Loss System Agree to Settle FTC Charges of Deceptive Claims

On April 21, 2017, the FTC announced the marketers of the NutriMost Ultimate Fat Loss System (NutriMost, LLC and NutriMost Doctors, LLC) agreed to settle charges they made false claims about the product.

February 09, 2017

Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products

On February 9, 2017, the FDA announced that VivaCeuticals Inc, doing business as Regeneca Worldwide, has been ordered by a federal court to stop selling its products, which were found to contain unsafe ingredients including DMAA.

September 16, 2015

Weight And Enhancement Supplement Recall Expanded

On September 11, 2015, One Minute Miracle Inc. issued a recall of all lots the following supplements which were found to contain undeclared drugs:

August 07, 2015

Male Enhancement and Weight Loss Supplement Containing Drugs Recalled

On August 6, 2015 Blue Square Market Inc. issued a recall of the following supplements which were found to contain undeclared drugs:

October 06, 2004

False Claims Made by Marketer of Cortisol-related Weight-Loss Supplements According to FTC

On October 6, 2004, the Federal Trade Commission (FTC)charged marketers of two dietary supplements with claiming, falsely and without substantiation, that their products can cause weight loss and reduce the risk of, or prevent, serious health conditions.

September 16, 2005

FTC Stops Weight-loss Claims about Seaweed-based Patches

On September 15, 2005, the U.S. Federal Trade Commission (FTC) announced that the alleged masterminds behind a fraudulent scheme to market two seaweed-based patches as weight-loss products to U.S. consumers have settled FTC charges.

August 31, 2007

FTC Stops Spammers Selling Bogus Hoodia and Human Growth Hormone

On August 23, 2007, the Federal Trade Commission (FTC), announced that spammers must stop sending unwanted and illegal e-mail messages about hoodia weight-loss products and human growth hormone anti-aging products the FTC alleges don't work.

March 19, 2009

QVC Settles Charges of False Claims for Supplements

On March 19, 2009, the Federal Trade Commission (FTC) announced that QVC, Inc., a TV home shopping channel and one of the world’s largest multimedia retailers, has agreed to pay $7.

November 03, 2011

Hoodia Marketers Fined and Banned from Business

On November 3, 2011, the Federal Trade Commission (FTC) announced that it settled charges brought against three people and two companies for deceptively advertising a supposed weight-loss supplement ingredient -- hoodia.

February 01, 2012

FDA Warns Seller of Almased Weight Loss Product of Marketing Violations

On January 18, 2011, the U.S. FDA sent a Warning Letter to Almased USA regarding legal violations in its marketing of its Almased product (Almased Synergy Diet).

November 09, 2012

FDA Warns Consumers of Two Weight Loss Supplements Containing a Drug

On November 8, 2012, the FDA warned consumers not to buy or use weight loss supplements Beautiful Body Slim and Japan Hokkaido Slimming Weight Loss Pills after FDA testing found these products contain the drug sibutramine.

January 11, 2013

Consumers May Be Eligible For Cold, Allergy and Weight Loss Supplement Refunds

On January 7, 2013, the Federal Trade Commission (FTC) announced that consumers who purchased the Iovate Health dietary supplements Accelis, nanoSLIM, Cold MD, Germ MD, or Allergy MD between January 2006 and July 2010 may qualify for a refund.

December 05, 2012

Hydroxycut Class Action Lawsuit To Be Settled

Iovate Health Sciences Inc. has agreed to a settlement of $25.3 million, pending final court approval, in a class action lawsuit that alleged the company deceived consumers about the safety of its Hydroxycut weight loss supplements.

February 15, 2013

FDA Seizes Weight Loss Supplements Containing Undeclared Drug

On Feb. 14, 2013, U.S. Marshals acting on behalf of the FDA seized weight loss supplements from Globe All Wellness, LLC which were found to contain the undeclared drug sibutramine hydrochloride.

June 20, 2014

FDA Warns Some Bee Pollen Products for Weight Loss Are Dangerous

On June 19, 2014, the FDA warned consumers that some weight loss products containing bee pollen have been found to contain hidden drugs.

May 20, 2014

FTC Charges Seller of Green Coffee Bean with False Weight Loss Claims, Fake Websites

On May 15, 2014, the Federal Trade Commission (FTC) filed a lawsuit against the sellers of Pure Green Coffee for making unsubstantiated weight loss claims and deceiving consumers with fake "news" websites.

December 16, 2013

Weight Loss Capsules Recalled Due Allergen Risk

On December 13, 2013, Stone Independent Research, Inc. issued recall of one lot of Zanocap Scientific Weight Loss 500 mg capsules because they contain undeclared whey protein, which is derived from milk.

December 06, 2013

Weight Loss Supplement Claims Challenged

On November 27, 2013, the National Advertising Division (NAD) recommended HealthyLife Sciences, LLC, modify or discontinue the use of certain claims made about the company's weight loss supplement Healthe Trim.

November 20, 2013

$2 Million In Weight Loss and "Fat-Burning" Supplements Seized

On November 12, 2013, U.S. Marshals seized more than $2 million worth of supplements from Georgia-based Hi-Tech Pharmaceuticals, Inc.

August 29, 2013

Seller of CELLFOOD Supplements Warned For Manufacturing Violations and Drug Claims

On August 1, 2013, the FDA issued a warning letter to supplement retailer Lumina Health Products, Inc.

August 08, 2014

Weight Loss Supplement Found to Contain DMAA Recalled

On August 6, 2014, Regeneca Worldwide issued a recall of two lots of appetite control supplement RegenESlim because FDA tests found them to contain DMAA (1,3-dimethylamylamine).

April 26, 2015

FDA Identifies More Products Listing Synthetic Amphetamine

On April 22, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called beta- methylphenylethylamine (BMPEA) on product labels.

April 11, 2015

Acai Berry Marketers Who Tricked Consumers with Fake News Sites Ordered to Pay $16 Million

On April 6, 2015, the Federal Trade Commission (FTC) announced that a recent U.S. district court ruling will require marketing affiliates for LeanSpa's acai berry and "colon cleanse" weight loss products to pay $16 million in consumer redress.

April 08, 2015

Does Your Weight Loss or Sports Supplement Contain Synthetic Amphetamine?

A study published on April 7, 2015, reported that among 21 weight loss, sports and cognitive enhancement supplements labeled as containing the plant extract Acacia rigidula, more than half were found to contain a synthetic, amphetamine-like compound called beta- methylphenylethylamine ...

April 10, 2021

Three More Male Enhancement Products Recalled Due to Undeclared Drugs

Between March 30 and April 5, 2021, three companies issued recalls of their male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.

April 02, 2021

Three Male Enhancement Products Recalled Due to Undeclared Drugs

Between March 24 and 26, 2021, three companies issued recalls of their male enhancement capsules because FDA analysis found them to contain sildenafil and tadalafil.

February 17, 2021

Adam’s Secret Male Enhancement Products Recalled Due to Undeclared Drugs

On February 15, 2021, adamssecret.co issued a recall of all lots of Adam's Secret Extra Strength 1500 and Adam's Secret Extra Strength 3000 male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.

January 20, 2021

Seller of Omega-3 Warned for Making Claims to Treat Focus, Mood

On December 9, 2020, the FDA issued a warning letter to Bodyhealth.com, LLC following a review of the company's website, which found statements made about the company's products Healthy-Thin Energize, Body Detox (Oral Spray), and Omega 3 Health to be drug claims.

December 13, 2021

Seller of Vitamin B12 Injections Without Prescription Pleads Guilty

On December 8, 2021, 46-year-old Des Moines resident Bradley Tomlinson plead guilty to a felony charge related to the sale of misbranded vitamin B12 injectable drugs. Tomlinson began selling these injectable drugs in May 2015 and marketed them as weight loss drugs.

January 12, 2021

Seller of Cholesterol, Weight Loss Products, and More Warned for Claims

On November 17, 2020, the FDA issued a warning letter to Bonagens following a review of the company's website, which found statements made about the company's products Anti-Aging Supports, Cholesterol & Diabetes Control, Gout Control, Hypertension Control, Liver Supports, Lungs ...

April 18, 2022

Moringa Concern: Blood Clots

A 63-year-old woman in New York with type 2 diabetes developed a blood clot in the lungs (i.e. pulmonary embolism) that her physicians suspect may have been caused by the use of a supplement containing Moringa oleifera extract (Ebhohon, Int J Emerg Med 2022).

June 16, 2004

FTC Challenges Ads for Kids’ Weight Loss Pill and Female Sexuality Supplement

On June 16, 2004 The Federal Trade Commission announced that it had charged three Florida-based companies and their principals with making false and unsubstantiated claims in connection with the advertising for “Pedia Loss,” a purported children’s weight loss product.

January 04, 2024

Toxic Herb Found in More Tejocote Root Supplements

On January 3, 2024, the FDA warned consumers not to purchase or use certain tejocote root supplements after FDA laboratory analysis confirmed the products contain yellow oleander (Thevetia peruviana), a toxic herb.

March 02, 2005

Marketer of Weight-Loss System Settles FTC Charges of Deceptive Advertising

On March 1, 2005, the Federal Trade Commission (FTC) announced that California infomercial producer Modern Interactive Technology, Inc.

December 22, 2008

FDA Warns Consumers About Tainted Weight Loss Pills

On December 22, 2008 the U.S. FDA alerted consumers not to purchase or consume any of more than 25 different products marketed for weight loss because they contain undeclared, active pharmaceutical ingredients that may put consumers’ health at risk.

August 30, 2015

Weight and Enhancement Supplements Recalled

On August 27, 2015, One Minute Miracle Inc. issued a recall of one lot each the following supplements which were found to contain undeclared drugs:

February 16, 2016

Work Out and Weight Supplements Contain Synthetic Amphetamine-Like Compound

On February 3, 2016, the FDA issued a warning letter to ATS Labs, LLC because labels for the company's work out and weight loss supplements CFI, Weapon-X Pre-Workout Extreme, and Lady Lean list a synthetic, amphetamine-like compound, 4-amino-2-methylpentane citrate (also called ...

March 15, 2016

FDA Warns Sellers of Weight and Workout Supplements Containing Acacia Rigidula

On March 7, 2016, the FDA issued warning letters to five sellers of supplements which were labeled as containing Acacia rigidula, an ingredient which is not permitted in dietary supplements.

April 16, 2016

Workout Supplement Containing Acacia Rigidula Recalled

On March 18, 2016, Nubreed Nutrition, Inc. issued a recall of all lots of its "pre-workout" supplement Undisputed which is labeled as containing Acacia rigidula, an ingredient which is not permitted in dietary supplements. 

April 08, 2016

Large Doses of Stimulant Methylsynephrine Found In Weight Loss Supplements

Amounts of methylsynephrine found in some supplements exceed prescription dosages, according to new study published in Drug Testing and Analysis.

April 06, 2016

FDA Warns of Stimulant Methylsynephrine In Supplements

On March 31, 2016, the FDA issued warning letters to seven companies selling products containing methylsynephrine (also called p-hydroxyephedrine or Oxilofrine), a stimulant drug which is not permitted in dietary supplements in the U.S.

October 13, 2017

Hi-Tech To Pay Over 40 Million to Settle FTC Charges of False Claims

On October 11, 2017, a U.S. District Judge ruled that Hi-Tech Pharmaceuticals Inc.

October 07, 2017

Weight Loss Supplement Recalled

On October 5, 2017, Kiriko, LLC recalled recalled all lots of A1 Slim 30 capsules after FDA analysis found the products to contain sibutramine, phenolphthalein and N-Desmethyl sibutramine.

November 25, 2016

DMAA Product Recalled

On November 23, 2016, NutriVitaShop (a dba of Naturecom Inc.) issued a recall of its DMAA net weight 500g because it may contain DMAA.

January 23, 2013

USPLabs Settles Class Action Lawsuit Over Controversial DMAA Ingredient

On December 18, 2012, a settlement was approved in the class action lawsuit against USPLabs, which alleged the company's use of the ingredient DMAA (1,3-dimethylamine) in the supplements OxyELITEPRO and Jacked3d was not safe or legal.

September 12, 2012

Distribution of Weight Loss Product Containing DMAA Should Be Stopped Immediately, Warns FDA

On August 28, 2012, the FDA issued a warning letter to Regeneca stating that the company's RegeneSlim, which was promoted as a dietary supplement for weight loss, is adulterated with dimethylamylamine (DMAA) and that failure to immediately cease distribution of this product could result in FDA ...

April 09, 2006

Sellers of Children’s Weight-Loss Product Settle FTC Charges

On April 6, 2006, the Federal Trade Commission (FTC) announced that the marketers of Pedia Loss, a purported children’s weight-loss product, and Fabulously Feminine, a supposed female libido enhancement product, had agreed to settle Federal Trade Commission charges that they made false and ...

April 29, 2015

FDA Targets Weight Loss and Workout Supplements Listing Synthetic Stimulant DMBA

On April 24, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called 1,3-dimethylbutylamine (DMBA) on product labels. 

April 14, 2015

Muscle Supplement Linked to Serious Liver Injury

On April 13, 2015, the FDA warned consumers not to use the muscle growth supplement Tri-Methyl Xtreme (distributed by Extreme Products Group) because it has been linked to serious liver injury.

November 11, 2014

Maker of Children's Vitamins, Weight Loss Supplements and More Warned for Manufacturing Violations

On October 30, 2014, the FDA issued a warning letter to VitalHealth Tech, Inc., following a facility inspection which found the company's products, including Kids Mighty Vites tablets, Omni Jr.

August 22, 2013

UK Warns Against a Weight Loss Supplement Still Available to Americans

The British government has identified the "fat-burner" supplement "I Force Dexaprine XR" as an unlicensed medical product and is instructing its retailer to remove it from the market, according to a report published in NutraIngredients.com.

September 27, 2013

Company Warned For Distributing Weight Loss Supplement Containing DMAA, Drug Claims

On September 6, 2013, the FDA issued a warning letter to Pure Energy Products, Inc., following a facility inspection which found that the company distributes a weight loss supplement, called obestrim, which contains dimethylamylamine, or DMAA.

June 23, 2013

Weight Loss Supplements Containing DMAA Recalled

On June 15, 2013, dietary supplement retailor Beta Labs, LTD issued a recall of certain lots of "fat burner" and weight loss supplements Oxyphen XR, Phentalene, Phen FX and Red Vipers because they contain 1,3-dimethylamylamine (DMAA).

January 31, 2014

Weight Loss Supplement Containing DMAA Recalled

On January 30, 2014, YoungYou International ("YoungYou") issued a voluntary recall of Mega Slim Herbal Appetite Management capsules because they were found to contain DMAA.

September 09, 2018

Higenamine -- A Potentially Dangerous Stimulant -- Found in Some Supplements

A recent study found concerningly high doses of the stimulant higenamine in some weight loss, energy and sports supplements sold in the U.S. Higenamine is a naturally-occurring stimulant which is permitted to be sold as a dietary supplement ingredient in the U.S.

January 24, 2020

Fat-Burning, Energy Supplement Linked to Heart Trouble

A 33-year-old woman in Australia developed cardiac ischemia (a lack of blood flow to the heart) after taking the "fat burning" supplement Alpha Lean-7, according to a recent report in the Journal of Sports Sciences.

June 16, 2020

NutraCap Labs Warned for Unsafe Ingredients and Manufacturing Violations

On May 21, 2020, the FDA issued a warning letter to NutraCap Labs LLC, which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.

April 03, 2014

Maker of Green Coffee Bean Extract and Weight Loss Supplement Warned for Manufacturing Violations

On March 13, 2014, the FDA issued a warning letter to Libi Labs, Inc.

October 21, 2014

Seller of Weight Loss, Saw Palmetto Supplements and More Warned for Drug Claims

On October 9, 2014, the FDA issued a warning letter to Bethel Nutritional Consulting, Inc., following a review of the company's website which found statements made about 15 Day Detox Diet, Alpha Lipoic Acid. 300 mg.

August 31, 2012

Energy, Fat Loss Supplement Recalled For Ephedrine Alkaloids

On August 28, 2012, dietary supplement re-sale distributor Brand New Energy (BNE) issued a recall of EphBurn 25 after FDA testing found the product to contain ephedrine alkaloids.

October 18, 2011

FDA Warns Consumers Against Eighteen Weight Loss Products Containing Drugs

On October 18, 2011, the U.S. FDA advised consumers not to purchase or use eighteen different weight loss products found to contain undeclared drug ingredients. The products are listed below with links to more detailed information and photographs.

March 09, 2004

FTC Stops False Advertising by Makers of Weight Loss and Arthritis “Cures”

On March 9, 2004, the Federal Trade Commission (FTC) announced that several direct mail marketers have agreed to pay $2.

July 15, 2010

Supplement Company Pays $5.5 Million to Settle False Advertising Claims

On July 14, 2010, the Federal Trade Commission (FTC), as part of its ongoing efforts to stop bogus health claims, announced that it is requiring a major marketer of dietary supplements to pay $5.

October 13, 2018

Pharmaceutical Drugs Found In Dietary Supplements Pose Danger to Consumers

Almost 800 dietary supplements sold between 2007 and 2016 contained unapproved pharmaceutical ingredients, according to a study published today in the Journal of the American Medical Association (JAMA).

December 26, 2023

Total Body Nutrition, TBN Labs, and Loud Muscle Science Banned from Selling Adulterated and Misbranded Dietary Supplements

On December 11, 2023, Total Body Nutrition LLC, TBN Labs LLC, and Loud Muscle Science LLC, as well as the companies’ owner, Mohammed Islam, were prohibited by federal court from manufacturing and distributing adulterated and misbranded dietary supplements.

July 09, 2010

FDA Issues Warning on Herbal Weight Loss Supplement

On July 8, 2010, the U.S. Food and Drug Administration (FDA) warned that Que She, marketed as an herbal weight loss supplement, contains active pharmaceutical ingredients not listed on the product label that could harm consumers, especially those with cardiovascular conditions.

November 15, 2009

Nationwide Recall of a Weight Loss Supplement Found to Contain Undeclared Drug Ingredients

On November 12, 2009, The U.S. Food and Drug Administration (FDA) announced that it informed GMP Herbal Products, Inc. that its product "Pai You Guo," a weight loss dietary supplement, contains undeclared drug ingredients.

March 08, 2012

Rx Drugs Found in Weight Loss and Enhancement Supplements

On February 6, 2012, FDA issued a letter to Globe All Wellness, LLC warning that two of their products contain undeclared prescription drugs.

October 24, 2012

FDA Warns Consumers of Weight Loss and Body Reshaping Supplements Containing Controlled Substance

On October 24, 2012, the FDA warned consumers not to purchase or use weight loss and body reshaping dietary supplement Zi Xiu Tang Bee Pollen Capsules (also referred to as Zi Xiu Tang Beauty, Face & Figure Capsules) because this product was found to contain sibutramine.

December 21, 2012

Weight Loss Supplement Containing Undeclared Drug Recalled

On December 19, 2012, P&J Trading issued a voluntary recall of SLIMDIA REVOLUTION after FDA testing found the dietary supplement contains undeclared sibutramine.

February 13, 2013

FDA Warns Maker of Weight Loss and Whey Protein Supplements For Manufacturing Violations and Misbranding

January 25, 2013, the FDA issued a warning letter to dietary supplement manufacturer SciLabs Nutraceuticals, following a facility inspection which found the company's dietary supplements and supplement ingredients, including N-Large 2, Flo-Gard AB, Nitrogen Glutamine capsules, Nutritech nutritional ...

April 12, 2013

FDA Warns Consumers About The Dangers Of DMAA

On April 11, 2013, the FDA warned consumers about the dangers of dietary supplements containing the ingredient 1,3-dimethylamylamine (DMAA).

August 15, 2002

FDA Warns Public About Chinese Diet Pills Containing Fenfluramine

On August 13, the U.S. FDA alerted the public about Chinese weight-loss products, Chaso (Jianfei) Diet Capsules and Chaso Genpi, because they pose a potential public health risk.

August 11, 2008

Stroke Attributed to Xenadrine Ephedra-Free Supplement

A case report in the journal Military Medicine (July 2008) attributes the occurance of vasospasm and stroke in a 36 year-old women to use of Xenadrine-EFX, a supplement used for weight loss.

February 29, 2008

FTC Sues Sellers of Weight-Loss Pills for False Advertising

On February 8, 2008 the The Federal Trade Commission (FTC) charged a business operation with violating federal law by falsely claiming that its weight-loss pills cause users to lose weight without dieting or exercise.

April 29, 2015

Teen Use of Weight Loss and Workout Supplements Labeled "For Adult Use Only" Concerning

Three new studies have raised concerns that teenagers are able to purchase "body-shaping" supplements, such as creatine, testosterone boosters, and "fat-burning" products from health food stores despite the fact that many of these supplements are labeled "for adult use only.

March 24, 2015

FTC Mails Refund Checks for Calcium Supplements

On March 18, 2015, the FTC announced 17,606 refund checks, totaling $954,828 were mailed to consumers who purchased the calcium supplement AdvaCAL (Lane Labs).

July 26, 2014

FTC Says Company Made "Outrageous" Weight Loss Claims

Marketers for the Canadian-based Freedom Center Against Obesity have agreed to pay $500,000 to settle FTC charges the company made deceptive claims about its Double Shot diet pills.

October 16, 2013

Methamphetamine-Like Compound Found In Popular Workout Supplement

A study published on October 14, 2013 (Cohen, Drug Test Analysis 2013) reports that the popular pre-workout energy supplement Craze (Driven Sports) has been found to contain the banned methamphetamine — like compound, N, á-diethylphenylethylamine.

September 02, 2016

Kratom To Be Classified a Schedule I Controlled Substance

On August 30, 2016, the U.S. Drug Enforcement Agency (DEA) announced its intent to classify the active compounds (mitragynine and 7-hydroxymitragynine) in kratom as Schedule I controlled substances.  

July 20, 2017

Jail Time for Seller of Spiked Supplements

On July 18, 2017, Derek Vest, the former president of Gentech Pharmaceutical located in Fort Meyers, Florida, was sentenced to 18 months in prison for introducing misbranded food into interstate commerce.

June 21, 2016

"Doctor Trusted" Seal and Certification Program for Dietary Supplements Misleading and Meaningless, Says FTC

SmartClick Media LLC, also doing business as Doctor Trusted, has agreed to settle Federal Trade Commission (FTC) charges that its "Doctor Trusted" seal and certificates, which appeared on some 800 websites promoting health products and dietary supplements, ...

March 02, 2016

Seller of Hoodia and Other Supplements Admits Fraud

On March 1, 2016, The United States Department of Justice announced that David Romeo, principal of several New Jersey- based dietary supplement companies, including Global Nutrients, Stella Labs and Nutraceuticals International, LLC, has pled guilty to conspiracy to distribute three kilograms or ...

September 30, 2015

Weight and Energy Supplement Contains Synthetic "Amphetamine"

On September 21, 2015, the FDA issued a warning letter to TruVision Health LLC. because the company's supplement tru Weight & Energy lists a synthetic, amphetamine-like compound, AMP (also called 1,3-dimethylbutylamine or DMBA) on product labels. 

January 11, 2023

Male Sexual Enhancement Supplement Found to Contain Prescription Drug

On January 9, 2022, the FDA issued a warning letter to Distributor RFR, LLC after laboratory analysis of the company’s SANGTER Natural Male Energy Supplement found the product to contain undeclared sildenafil, a prescription medication.

January 16, 2018

Marketers of CellAssure and Cognify Settle FTC Charges of Deceptive Cancer Claims

On January 11, 2018, the FTC announced that CellMark Biopharma, LLC and its CEO, Derek E.

January 19, 2022

FDA Warns Seller of Carnitine and Alpha Lipoic Acid Supplements

On November 18, 2021, the FDA issued a warning letter to GeroNova Research Inc.

April 05, 2022

Sexual Enhancement Capsules for Men Recalled

On April 1, 2022, F&S Medical Supply, dba Pink Toyz, recalled one lot of Pink Pussycat 3000 mg capsules to the consumer level because FDA analysis found them to contain sildenafil.

May 09, 2022

Natural Organics Keto Capsules Recalled Due to Gluten

On March 6, 2022, Natural Organics, Inc. issued a recall of four lots of NaturePlus Keto Living Sugar Control Capsules that were found to contain gluten.

July 06, 2022

FDA Warns Kratom Companies for Arthritis, Pain Relief Claims & More

On January 30, 2022, the FDA issued warning letters to four sellers of kratom products because they were promoted to treat pain relief, opioid withdrawal, blood sugar control, anxiety, and to treat rheumatoid arthritis.

July 13, 2022

FDA Warns Sellers of Tainted Honey-Based Sexual Enhancement Products

On July 12, 2022, the FDA issued warning letters to four companies selling honey-based products promoted for sexual enhancement after tests conducted by the FDA found the products to contain the prescription drugs Tadalafil and Sildenafil.

July 15, 2022

Honey-Based Enhancement Supplement Recalled

On July 13, 2022, Shopaax.com issued a recall of all lots of its honey-based sexual enhancement product, Kingdom Honey Royal Honey VIP, after FDA analysis found the presence of undeclared sildenafil.

July 26, 2022

Sexual Enhancement Supplement Sold on Amazon Recalled

On July 21, 2022, Ultra Supplements LLC issued a recall of one lot of Sustango capsules after Amazon laboratory analysis found the presence of the prescription drug Tadalafil. The company has received no reports of adverse effects related to this recall to date.

August 03, 2022

Sexual Enhancement Supplement Recalled Due to Sildenafil

On August 1, 2022, DISTRIBUTOR RFR, LLC recalled one lot of SANGTER Energy Supplement 3000 mg to the consumer level after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

November 17, 2022

FDA Warns Consumers Not to Use Male Enhancement Supplement

On November 10, 2022, the FDA warned consumers not to buy or use Sangter Natural Male Energy Supplement after FDA laboratory analysis confirmed the presence of undeclared sildenafil.

November 21, 2022

6 Supplement Companies Warned by FDA for Making Cholesterol Claims

On May 4, 2022, the FDA issued warning letters to six supplement companies following review that found statements made on company websites and Walmart purchase pages suggesting the products could lower cholesterol to be drug claims, which are not permitted for dietary supplements.

June 16, 2022

Omega 3 Supplements Recalled Due to Undeclared Drug Ingredients

On May 28, 2022, Latin Foods Market issued a voluntary recall of one lot of Artri King Reforzado con Ortiga y Omega 3 tablets after FDA laboratory analysis found the presence of undeclared diclofenac and dexamethasone.

December 01, 2017

Health Research Labs Agrees to Settle FTC Charges of False Claims, Deceptive Marketing of BioTherapex and NeuroPlus

On November 30, 2017, the FTC announced Health Research Laboratories LLC and owner, Kramer Duhon, agreed to settle charges that they made false claims about the company's products, BioTherapex and NeuroPlus.

July 26, 2013

Safety of Certain Weight Loss and Bodybuilding Supplements Called Into Question

On July 25, 2013, USA Today reported that several supplements, including weight loss, body building and sports nutrition supplements, have come under scrutiny after being found to contain illegal ingredients, or were associated with failed drug tests and adverse events.

March 13, 2015

Three Weight Loss Supplements Found to Contain Drugs

The FDA recently warned consumers not to buy or use the following weight loss supplements because they were found to contain undeclared drugs. Each was identified during an examination of international mail shipments.

April 02, 2004

Makers of Fat and Starch "Blockers" Receive FDA Warning Letters

On April 1, 2004, the Food and Drug Administration (FDA)announced that it had sent warning letters to 16 dietary supplement distributors making false and misleading claims for weight loss products promoted over the internet.

February 01, 2013

DMAA Supplement Linked to Runner's Death

The cause of death of London marathon runner Claire Squires has been ruled by the investigating coroner as cardiac failure due to extreme exertion, complicated by DMAA toxicity.

November 08, 2012

FDA Warns Consumers of "Slimming Coffee"

On November 8, 2012, the FDA warned consumers not to purchase or use Best Share Green Coffee: Brazilian Slimming Coffee after FDA testing revealed the coffee, which was promoted for weight loss, contains the drug sibutramine.

November 02, 2008

Sales of Weight-Loss Supplement Suspended -- May Contain Diuretic Drug

On October 31, 2008, Associated Press reported that makers of the weight loss supplement StarCaps have suspended sales following accusations that the product contains a non-listed pharmaceutical diuretic, Bumetanide.

January 31, 2012

FTC Stops Fake News Sites About Acai Berry Products

As published on the U.S. Federal Trade Commission's (FTC) website on January 25, 2011, six online marketers settled with the FTC to stop posting fake news on websites intended to promote acai berry supplements and other weight-loss products.

October 05, 2012

Illegal Claims on Weight Loss, Immune System Dietary Supplements, and Few Backed by Clinical Data

On October 3, 2012, the U.S. Department of Health and Human Services issued a report warning that dozens of weight loss and immune system supplements have illegal claims of curing or treating disease on their labels and/or lack the scientific evidence to support such label claims.

January 04, 2012

Seller of "HCG Drops" for Weight Loss Warned by FDA and FTC of Violations

On December 21, 2011, the U.S. FDA and FTC sent a joint Warning Letter to hCG Drops LLC regarding its marketing of Slim Diet Drops. According to the letter, the product is considered an unapproved drug because it is promoted for drug-like uses on the company's website, including the following:

June 23, 2020

BioPure Healing Products Warned for Manufacturing Violations

On June 17, 2020, the FDA issued a warning letter to BHP Holdings Inc.

June 23, 2020

FTC Sends Refund Checks to Consumers of Deceptive "Free Trial" Scheme

On June 22, 2020, the FTC announced it is mailing 187,425 checks totaling more than $8.

November 20, 2020

FTC Files Complaint Against Two Supplement Companies for Deceptive Marketing

On November 20, 2020, the FTC approved a Part 3 administrative complaint against Health Research Laboratories, LLC, its owner Kramer Duhon, and Whole Body Supplements, LLC for making unverified claims that their products can prevent or treat diseases.

June 02, 2020

FTC Sends Refund Checks for "ReJuvination" Supplement

On June 1, 2020, the FTC announced it is mailing 1,310 checks totaling nearly $149,000 to consumers who purchased ReJuvination, a product deceptively marketed as a cure-all for various age-related conditions, including cell damage, heart attack damage, brain damage, and deafness.

May 30, 2020

FTC Sends Refund Checks for TrueAloe and AloeCran

On May 26, 2020, the FTC announced it is mailing 22,581 checks totaling more than $470,000 to consumers who purchased deceptively marketed supplements, TrueAloe and AloeCran.

July 12, 2023

FDA Warns Company for Promoting Kratom Products for Pain, Mood, and More

On July 3, 2023, the FDA issued a warning letter to Sunshine Trading Company, Inc.

January 20, 2021

FDA Warns Seller of Vitamin D, Curcumin and CoQ10 Promoted for Treating COVID-19

On December 28, 2020, the FDA issued a warning letter to Smarter Nutrition, Inc. following a review of the company's website, which found statements made about the company's products Smarter Curcumin, Smarter Ubiquinol, and Smarter Vitamin D3 to be drug claims.

February 02, 2021

Seller of Aloe Products Warned for Claiming to Treat Joint Stiffness

On January 22, 2021, the FDA issued a warning letter to American Global Health Group, LLC following a review of the company's website, which found statements made about the company's products AloeCure VeraFlex, AloeCure Advanced Formula Capsule, AloeCure Pure Aloe Vera ...

February 02, 2021

FDA Warns Seller of Reishi Mushroom Supplements

On January 6, 2021, the FDA issued a warning letter to Entia Biosciences, Inc following a review of the company's website, which found statements made about the company's products Lion's Mane - All Natural Supplement, Antrodia Mushroom Powder, Maitake Mushroom Powder, Reishi ...

February 02, 2021

FDA Warns Seller of Ginger, Echinacea, and More

On December 10, 2020, the FDA issued a warning letter to Prairie Dawn Herbs following a review of the company's website, which found statements made about the company's products Chest Tea, Ginger Oil, Dandelion root Tincture, Echinacea purpurea Tincture, Antispasmodic Tincture, ...

January 21, 2021

Federal Court Bars Fusion Health From Promoting Vitamin D for COVID-19

On January 8, 2021, the United States Department of Justice announced a permanent injunction has been entered, barring dietary supplement marketer Matthew Ryncarz and his companies Fusion Health and Vitality LLC dba Pharm Origins and Fusion Ionz LLC dba Pharm Origins from making claims that their ...

July 20, 2021

Alpha Male Plus Recalled

On July 16, 2021, Alpha Male Plus issued a recall of Alpha Male Plus Male Enhancer fruit chews because FDA analysis found them to be contaminated with tadalafil.

May 24, 2021

U.S. Marshals Seize $1.3 Million Worth of Kratom

U.S. Marshals have seized approximately $1.3 million worth of bulk kratom and kratom supplements manufactured by Atofil, LLC, a subsidiary of Premier Manufacturing Products, according to the FDA.

April 17, 2021

NS NY Distributor Inc Male Enhancement Products Recalled Due to Undeclared Drugs

On April 8, 2021, NS NY Distributor Inc issued a recall of all lots of Premium Orgazen 7000 and Ginseng Power 5000 male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.

June 02, 2022

Walmart Inc. Recalls Joint Supplements With Omega-3, Glucosamine & Curcumin

On May 28, 2022, Walmart Inc. issued a voluntary recall of all lots of Artri Ajo King Joint Supplements after FDA laboratory analysis found the presence of undeclared diclofenac.

December 06, 2011

FTC Stops Operator of Fake News Sites Offering Acai and Colon Cleanse Products

On December 1, 2011, The Federal Trade Commission announced that it has filed a complaint jointly with the State of Connecticut, seeking to permanently stop a Connecticut-based operation that allegedly used fake news websites to promote their products, made deceptive weight-loss claims, and told ...

September 23, 2014

Maker of Joint and Weight Products Warned for Hidden Drugs, Manufacturing Violations

On September 15, 2014, the FDA issued a warning letter to West Coast Laboratories, Inc., because the company's joint health supplements, Super ArthGold and Pro ArthMax, were found to contain hidden drugs.

June 12, 2014

Marketers of Memory Supplement Settle FTC Charges of Deceptive Claims

Martek Biosciences Corporation and i-Health Inc., marketers of BrainStrong Adult, have agreed to settle Federal Trade Commission (FTC) charges that claims the supplement could improve adult memory and prevent cognitive decline were deceptive, and not supported by sufficient clinical evidence.

April 18, 2014

FDA Questions Ingredient in Workout Supplement

On April 4, 2014, the FDA issued a warning letter to Driven Sports Inc., following a label review which found the company's workout supplement, CRAZE, to be adulterated because it contains the new dietary ingredient Dendrobex.

July 24, 2013

USPLabs Destroys $8 Million Worth of Supplements Containing DMAA

On July 16, 2013, the FDA announced that USPLabs voluntarily destroyed its inventory of OxyElite Pro and Jack3d, workout supplements that contain DMAA. DMAA has been linked to a number of adverse effects and is not allowed to be sold as a dietary supplement ingredient.

September 05, 2013

Seller of Herbal Supplements and "Tonics" Warned For Manufacturing Violations and Drug Claims

On May 24, 2013, the FDA issued a warning letter to Sundial Herbal Products following a facility inspection which found the company's products, including Woman Back Tonic, Koromantee, Wood and Root Tonic, Arthritis, Asthma, Diabetics, Sundial Ashanti Weight Loss Energy Lifter, Appetite Suppresser, ...

August 16, 2013

Maker of Energy, Weight Loss, Sleep and Vitamin D Supplements Warned for Manufacturing Violations

On July 22, 2013, the FDA issued a warning letter to N.V.E. Pharmaceuticals, Inc.

November 20, 2013

Another Meth-Like Compound Discovered In Weight Loss Supplements

A "non-natural" amphetamine-like compound, identified as beta-methylphenethylamine, was discovered in nine supplements recently tested by FDA scientists.

May 20, 2015

Supplements to Eliminate Gray Hair Not Supported by Science, Says FTC

On May 13, 2015, the FTC announced marketers of GetAwayGrey and Rise-N-Shine, dietary supplements promoted to reverse or prevent gray hair, have agreed to settle charges that claims made about the products are not supported by science.

May 16, 2015

FTC Mails Refund Checks to Nopalea Consumers

On May 15, 2015, the FTC announced it is mailing almost 500,000 checks totaling approximately $3 million to consumers who purchased the cactus-based fruit drink Nopalea (TriVita Inc).

July 26, 2014

Marketers of Nopal Cactus Drink Settle FTC Charges of Deceptive Claims

TriVita Inc., and marketers of the company's "prickly pear" fruit drink Nopalea have agreed to pay $3.5 million in consumer refunds to settle FTC charges they made deceptive claims that the drink treats health problems ranging from skin conditions to joint pain and respiratory problems.

September 30, 2014

U.S. Marshals Seize $5 Million Worth of Kratom

On September 25, 2014, U.S. Marshals seized more than 25,000 pounds of raw kratom valued at over $5 million from Rosefield Management, Inc. in Van Nuys, California. The action was taken at the request of the FDA.

December 30, 2014

Maker of Aloe, Weight Loss Supplements and More Warned for Manufacturing Violations, Drug Claims

On December 17, 2014, the FDA issued a warning letter to Dandy Day Corporation, following a facility inspection which found the company's products, including Aloe Pearl, Alfalo, Aloespring, Crave Away, Original Supreme Energy, Ener "G," Can G, Flora G, Flora G Plus, and Garolic, to be adulterated ...

February 06, 2015

POM Wonderful Claims Were Deceptive, Court Rules

On January 30, 2015, the Federal Trade Commission (FTC) announced that an appeals court has upheld the Commission's ruling that marketers for POM Wonderful made deceptive health claims about the product.

February 25, 2011

Weight Supplement Found by FDA to Contain Prescription Drug

The U.S. FDA posted an announcement (dated February 9, 2011) by Svelte 30 Nutritional Consultants indicating that a sample of Svelte 30 orange & gray capsule was collected and tested by FDA in January 2011.

January 04, 2011

Weight Loss Supplement Containing a Drug Can Cause Serious Adverse Events, Warns FDA

On December 31, 2010 the U.S. FDA warned consumers not to use Fruta Planta weight loss products because they contain sibutramine, a drug withdrawn from the market in December 2010 for safety reasons.

July 19, 2010

FDA Warns of Drug in Herbal Slimming Supplement

On July 19, 2010, the U.S. FDA issued a safety warning to consumers regarding Slim-30 Herb Supplement. FDA analysis of the product found it to contain undeclared N-Desmethyl Sibutramine and traces of Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss.

December 08, 2009

Warning on Acai Berry Supplements Spiked with Drug

On December 8, 2009, Health Canada (the Canadian health agency) advised consumers not to use certain Acai Berry products after a large number of shipments of adulterated products were stopped at the border.

February 20, 2013

FDA Warns USPLabs For Adulteration and Drug Claims

On December 4, 2012 the FDA issued a warning letter to USPLabs, LLC following facility inspections which found the company's products, including dietary supplements Jacked3d, OxyElite Pro, Prime, and Super Cissus, to be adulterated because they were prepared, packed, or held under conditions that ...

January 24, 2013

"Thermo Stimulating" Supplement Recalled -- Contained DMAA

On January 23, 2013, Health Canada advised consumers not to use certain batches of Muscletech Hydroxystim capsules which were found to contain DMAA (1,3-dimethylamylamine) and have been recalled by their distributor.

November 12, 2017

Weight Loss and Cleanse Supplements Contain Adulterated and Improperly Labeled Ingredients, FDA Warns

On November 2, 2017, the FDA issued a warning letter to Create-A-Pack Foods, Inc.

October 11, 2016

Seller of Glucosamine and Chondroitin Settles FTC Charges of False Advertising

On October 5, 2016, the FTC announced the sellers of the liquid glucosamine and chondroitin supplement Supple (Supple LLC) agreed to settle charges they made false claims about the product.

October 01, 2016

No Evidence Supplement Can Reverse or Prevent Gray Hair, Says FTC

On September 23, 2016, the FTC announced a U.S. district court has issued a judgement prohibiting the makers of Grey Defence dietary supplements from making claims the products can reverse or prevent grey hair, unless they are not misleading and are supported by reliable scientific evidence.

October 17, 2015

23,000 ER Visits Linked to Supplements: Palpitations, Swallowing Problems, Allergies Common

Approximately 23,000 emergency room visits per year are attributed to adverse events linked to the use dietary supplements, according to a large, long-term study by the FDA and the Centers for Disease Control and Prevention (CDC).

August 22, 2015

Synthetic Amphetamine, Less Protein and More Sugar Than Claimed Found in Workout Supplements

On August 7, 2015, the FDA issued a warning letter to New Dawn Nutrition, Inc.

July 12, 2015

Marketers of Memory Supplement to Pay $1.4 Million to Settle FTC Charges

On July 8, 2015, the FTC announced the marketers of Procera AVH (Brain Research Labs Inc.) have agreed to pay $1.4 million to settle charges they made deceptive claims that the supplement could significantly improve memory, mood and cognitive function.

January 12, 2016

Over $400,000 Worth of Kratom Supplements Seized by U.S. Marshals

On January 6, 2016, U.S. Marshals seized nearly 90,000 bottles of dietary supplements labeled as containing kratom (brand name RelaKzpro) valued at over $400,000, from Dordoniz Natural Products LLC in South Beloit, Illinois. The action was taken at the request of the FDA.

February 03, 2016

Seller of Weight and Enhancement Supplements Warned For Drug Claims

On December 11, 2015, the FDA issued a warning letter to The One Minute Miracle, Inc., following a review of the company's website which found statements made about   Miracle Diet 30 and Miracle Rock 48 to be drug claims.

January 21, 2016

Morphine Found in Licorice Product

On January 20, 2016, Master Herbs, Inc. issued a recall of all lots of Licorice Coughing Liquid because it was found to contain morphine.

August 05, 2016

U.S. Marshals Seize $150,00 Worth of Kratom

On August 4, 2016, the FDA announced that U.S. Marshals seized approximately $150,000 worth of dietary supplements labeled as containing kratom from Nature Therapeutics (dba Kratum Therapy). The action was taken at the request of the FDA.

April 05, 2016

Muscle Enhancement Supplement Recalled

On April 5, 2016, Invisiblu International LLC issued a recall of one lot of the muscle enhancement supplement Continuum Labs LGD-Xtreme because it contains LGD-4033 Ligandrol. The risks of this ingredient are not known.

May 12, 2020

FTC Halts Deceptive Supplements & Cosmetics "Free Trial" Scheme

On May 8, 2020, the owners of AH Media Group, LLC agreed to halt their allegedly deceptive practice of luring consumers with supposed "free trial" offers for cosmetics and dietary supplements, then enrolling them in subscriptions and billing them without their consent.

October 12, 2020

NutraClick to Pay $1.04 Million for Illegally Billing Consumers

On September 22, 2020, the Federal Trade Commission (FTC) announced that NutraClick LLC agreed to pay $1.04 million to settle FTC charges that the company was deceptively selling and billing consumers for supplements and beauty products.

November 24, 2020

Recalled Vitamin D Contains Potentially Dangerous Ingredient

On November 22, 2020, Fusion Health and Vitality LLC recalled all 2020 lots of CORE Essential Nutrients and Immune Boost Sublingual Vitamin D3 because they are adulterated. CORE Essential Nutrients contains the unapproved food additive hordenine HCl.

June 05, 2020

Seller of CBD, Sleep Aids, and Cold & Flu Products Warned for Manufacturing Violations

On April 28, 2020, the FDA issued a warning letter to The Dragontree Apothecary LLC, which found the company's Sleep Support, Anxiety Relief, Cold & Flu Relief, and Inflammation Relief to be adulterated because they were prepared, packed, or held under conditions that ...

June 02, 2020

Sundial Herbal Ordered to Halt Distribution of Products

On June 1, 2020, a New York federal judge filed an order against two individuals doing business as Sundial Herbal Products to stop the company from distributing its products, which were found to be misbranded and promoted as drugs.

February 26, 2020

Company Failed to Report Adverse Events Associated With Its Nutrition Shakes

On February 12, 2020, the FDA sent a warning letter to Market America Inc for failure to submit serious adverse event reports about two of its products, as required by federal regulation. The company received two reports following serious adverse events but did not submit the proper forms:

June 04, 2004

FTC Charges Marketers of Two Supplements with False Claims to Cure Range of Diseases

On June 3, 2004 the Federal Trade Commission (FTC) charged marketers of two dietary supplements with falsely claiming that their products can prevent and cure cancer and other diseases. According to the FTC’s complaint, Boston-area marketers Direct Marketing Concepts, Inc. (DMC), ITV Direct, Inc.

June 09, 2005

FTC Cracks Down on "HGH" Supplements; $20 Million in Consumer Redress

On June 9, 2005, The Federal Trade Commission (FTC) announced that two Florida businesses have agreed to a federal court order requiring them to pay up to $20 million in consumer redress – the largest monetary judgment ever obtained in an FTC health fraud case – to settle charges that they ...

March 19, 2007

Canada Warns of Weight Loss Supplement with Rx Drug

On March 14, 2007, Health Canada advised consumers not to use MIAOZI Slimming Capsules because they have been found to contain sibutramine, a prescription medication that should only be taken under medical supervision.

October 12, 2005

Supplement Company to Pay $2 Million Penalty For Alleged Violations of FTC Order

On October 12, 2005 the Federal Trade Commission (FTC) announced that under the terms of a consent decree approved by the it for submission by the U.S. Department of Justice (DOJ) to the federal court for approval, NBTY, Inc. (NBTY, formerly Nature’s Bounty, Inc.

October 10, 2003

Government Stops Sale of Supplements Claiming to Treat Obesity and Impotence

On October 8, 2003, The Food and Drug Administration (FDA) announced that on September 22, 2003, U.S. District Court Judge Robert J. Vining, Jr.

March 01, 2013

Manufacturer of Joint, Weight Loss, Muscle Supplements and More Warned for Adulteration, Misbranding and Drug Claims

On February 4, 2013, the FDA issued a warning letter to DC Nutrition, Inc.

August 01, 2013

Fat Loss and Muscle Enhancement Supplements Found To Contain DMAA

On June 17, 2013, the FDA issued a warning letter to Formulife, Inc., dba Purus Labs, Inc., following a facility inspection which found the dietary supplements Fat Smack XR Thermolipolytic, Muscle Marinade Fresh Fruit and Muscle Marinade Cherry Limeade to contain DMAA.

October 28, 2015

GNC Accused of Selling Supplements with Unlawful Ingredients

On October 22, 2015, Oregon Attorney General Ellen Rosenblum filed a lawsuit against supplement retailer GNC, alleging that the company sold products that were adulterated with BMPEA and picamilon, which are not lawful dietary supplement ingredients.

November 26, 2019

FDA Warns Companies Selling CBD Products as Dietary Supplements

On November 25, 2019, the FDA issued warning letters to 15 companies for selling products containing CBD (cannabidiol) labeled and marketed as dietary supplements, and/or for making drug claims about these products.

September 03, 2019

Federal Court Shuts Down Two Supplement Companies Selling Weight, Joint Health and Other Supplements

On September 3, 2019, a U.S. District Court entered a consent decree of permanent injunction against Basic Reset and Biogenyx, two Tennessee-based companies that sell dietary supplements and other product promoted for health benefits.

June 03, 2019

Vinpocetine May Cause Miscarriage or Fetal Harm

Women who are pregnant or who could become pregnant should not take Vinpocetine because it may cause miscarriage or harm fetal development, the FDA warned in a news release today.

April 16, 2019

DMHA and Phenibut Are Not Permitted in Dietary Supplements, Warns FDA

On April 16, 2019, the FDA announced it has issued 11 warning letters to companies whose dietary supplement products contain the drugs DMHA or phenibut, and therefore are in violation of the law.

April 12, 2019

CDC: Kratom Linked to 91 Deaths

Kratom may have played a role in twice as many deaths as has been previously estimated, according to a report issued today by the Center of Disease Control (CDC).

June 20, 2020

FTC Warns 30 More Companies for Coronavirus Claims

On June 18, 2020, the FTC announced that it sent warning letters to 30 companies for selling products such as immune system boosters, colloidal silver, vitamin C, and CBD with unsupported claims that they can treat coronavirus (COVID-19).

March 04, 2003

U.S. Warns of Ephedra Risks and Proposes Warning Label for Supplements

On February 28, the Department of Health and Human Services (HHS) announced a series of actions designed to protect Americans from potentially serious risks of dietary supplement products containing ephedra.

January 11, 2002

Canada Requests Recall of Certain Ephedra/Ephedrine Products

OTTAWA - January 10, 2002 - Health Canada is requesting a recall from the market of certain products containing Ephedra/ephedrine after a risk assessment concluded that these products pose a serious risk to health.

October 06, 2005

Deceptive Marketing of “Supreme Greens" -- Settlement with FTC

On October 6, 2005, the Federal Trade Commission (FTC) announced that three individuals and two companies have settled FTC charges over their roles in the deceptive marketing of Supreme Greens, an herbal supplement.

September 23, 2005

FTC Continues Litigation Against Makers of CortiSlim and CortiStress Supplements

On September 21, 2005 the Federal Trade Commission (FTC) announced that three defendants will give up $4.

January 17, 2006

FDA Warns Consumers about Brazilian Diet Pills Found to Contain Active Drug Ingredients

On January 13,2006, the U.S. Food and Drug Administration (FDA) warned consumers not to use two unapproved drug products that are being marketed as dietary supplements for weight loss.

June 25, 2019

Kratom Is Dangerous and Not Proven to Treat Addiction, FDA Warns Marketers

On June 25, 2019, the FDA issued warning letter to two marketers and distributors of kratom products, listed below, for illegally selling unapproved, misbranded kratom-containing drug products with unproven claims about their ability to treat or cure opioid addiction and withdrawal symptoms.

February 06, 2018

FDA Links 44 Deaths to Kratom

On February 6, 2018, FDA announced it is now aware of 44 deaths associated with the use of kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms. This is an increase from the 36 deaths associated with kratom that the agency reported in November 2017.

July 10, 2018

Blissful Remedies Kratom Recalled Due to Salmonella Risk

On June 30, 2018, Blissful Remedies issued a recall of three kratom products because they have the potential to be contaminated with Salmonella.  

April 21, 2018

NxtGen Botanicals Maeng Da Kratom Recalled

On April 18, 2018, NGB Corp. of West Jordan, Utah issued a recall of NxtGen Botanicals Maeng Da Kratom labeled bottles of encapsulated product because they have the potential to be contaminated with Salmonella. To date, one illness has been reported to the FDA.

April 09, 2018

Kratom Powders and Capsules Recalled Due to Salmonella Risk

On April 5, 2018, Club 13 issued a recall of certain kratom powders and capsules because they have the potential to be contaminated with Salmonella.

September 19, 2018

Seller of Curcumin, Garcinia, Glucosamine and More Warned for Manufacturing Violations

On September 7, 2018, the FDA issued a warning letter to Best Nutrition Products, Inc.

November 27, 2018

More Dog Food Recalled Due to Risk of Vitamin D Toxicity

On November 27, 2018, Sunshine Mills, Inc. issued a recall of select Evolve Puppy, Sportsman's Pride Large Breed Puppy and Triumph Chicken and Rice Dog Food because they may contain elevated levels of vitamin D.

November 27, 2018

High Levels of Lead Found in Kratom Products

Some kratom products contain levels of lead and nickel that are not considered safe for human consumption, according to tests conducted by the FDA.

November 06, 2018

Dog Food Recalled After Reports of Vitamin D Toxicity

On November 2, 2018, Natural Life Pet Products and Nutrisca issued a recall of certain dry dog foods because they contain elevated levels of vitamin D. The elevated levels of vitamin D were found during an investigation into several reports of vitamin D toxicity by pet owners.

June 19, 2023

A&Z Pharmaceutical Warned for Promoting Calcium & Vitamin D for Hair Loss, Osteoporosis & Cancer

On June 1, 2023, the FDA issued a warning letter to A&Z Pharmaceutical, Inc. following inspection of the company’s website and social media, which found statements about the company’s Chewable Calcium 600MG with Vitamin D for Kids in Orange Flavor products to be drug claims.

September 24, 2024

Supplement for Eczema Recalled

On September 18, 2024, 123Herbals LLC issued a recall for all lots of Vail-Bon Jie Yang Wan capsules, which are promoted to treat eczema and other skin conditions, because they contain undeclared dexamethasone and chlorpheniramine.

August 05, 2016

Seller of Fertilix Warned By FDA

On July 22, 2016, the FDA issued a warning letter to CellOxess LLC, following a review of the company's websites, social media pages and marketing literature which found statements made about Fertilix Preconceptual, Fertilix Low Dose and Fertilix Max to be drug claims.

July 23, 2016

Seller of GlucoCor Warned for Drug Claims

On June 30, 2016, the FDA issued a warning letter to MC-COR, LLC, following a review of the company's website and Facebook page which found statements made about its GlucoCor capsules to be drug claims.

October 01, 2016

Homeopathic Teething Tablets and Gels May Pose Danger, FDA Warns

On September 30, 2016, the FDA warned consumers that homeopathic teething tablets and gels may be dangerous for infants and children. The agency has received adverse events reports, including seizures, associated with the use of these products.

November 01, 2017

FDA Warns Sellers of Bodybuilding Supplements Containing Steroid-Like Substances

On October 23, 2017, the FDA issued warning letters to three supplement distributors because several of their bodybuilding products contain selective androgen receptor modulators (SARMs).

October 06, 2006

FDA Warns Mangosteen Juice Maker of Drug Promotions

On September 20, 2006, the U.S. Food and Drug Administration (FDA) sent a Warning Letter to the makers of Xango, a mangosteen juice product. The letter advised that distributors of the product were using brochures making health claims restricted to the promotion of drugs.

June 20, 2003

FTC Charges Marketers of Seasilver with False and Deceptive Claims

On June 19, 2003, The Federal Trade Commission (FTC) and the Food and Drug Administration (FDA) announced coordinated actions against two companies - both charged with promoting the dietary supplement "Seasilver" with unsubstantiated medical claims. The agencies' actions against Seasilver USA, Inc.

September 08, 2012

Medifast Settles False Advertising Suit

On September 7, 2012, Jason Pharmaceuticals Inc., a wholly owned subsidiary of Medifast, agreed to pay a $3.7 million civil penalty and meet new compliance requirements as part of a settlement with the U.S. Department of Justice and the Federal Trade Commission.

October 08, 2010

"Red Flags" for Spotting Tainted Supplements

In recent years, the FDA has identified hundereds of products marketed as dietary supplements or conventional foods with hidden drugs and chemicals. In reaction to this, the FDA recently created a flyer to help retailers spot questionable products. ConsumerLab.

September 13, 2010

Recall of Herbal Slimming Supplement Spiked with Drug

The U.S. FDA posted a notice dated August 18, 2010 indicating that Slim-30 Herbal Supplement (Lot 6032101) has been recalled by its distributor, J & H Besta Corp.

November 28, 2008

Fat Loss Supplement Recalled for Containing Prescription Drug

On November 26, 2008, the FDA reported that Zhen De Shou Fat Loss Capsules are being recalled by the distributor, Fashion Sanctuary. FDA analysis found the product to contain undeclared sibutramine, an FDA approved drug used as an appetite suppressant for weight loss.

April 23, 2009

Recall of "Slimming" Supplements Spiked with Drug

On April 20, 2009 the U.S. FDA reported a nationwide recall of dietary supplements distributed by Universal ABC Beauty Supply International.

October 25, 2013

Supplement Company Warned For Numerous Manufacturing Violations

On August 2, 2013, the FDA issued a warning letter to DNE Nutraceuticals, Inc., following a facility inspection which found the company's products to be adulterated because they were packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.

December 19, 2013

Maker of Joint Health Supplements Warned for Manufacturing Violations

On December 4, 2013, the FDA issued a warning letter to PurQuality, LLC.

March 19, 2014

Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations

On September 19, 2013, the FDA issued a warning letter to Herbalist and Alchemist, Inc.

August 12, 2024

FDA Warns "Apricot Power" Apricot Seeds Contain Toxic Compound

On May 24, 2024, the FDA warned consumers not to consume three Apricot Power bitter apricot seed products because they were found to contain the toxic compound amygdalin.

February 05, 2019

Hill's Science Diet, Prescription Diet Dog Food Recalled Due to Risk of Vitamin D Toxicity

Recall Expanded (3/20/19): This recall was expanded to include additional products.

December 19, 2024

Gout and Arthritis Supplement Recalled Due to Undeclared Drugs

On December 12, 2024, Buy-herbal recalled all lots of Nhan Sam Tuyet Lien Truy Phong Hoan capsules within expiry after FDA testing found them to contain undeclared furosemide, dexamethasone and chlorpheniramine. These drugs are not permitted in dietary supplements.

February 06, 2023

Recalled Eye Drops Linked to Vision Loss and One Death

On February 2, 2023, Global Pharma Healthcare issued a nationwide recall of its Artificial Tears Lubricant Eye Drops due to potential contamination with bacteria that can cause serious infection, blindness, and death.

September 12, 2018

FDA Urges Consumers to Avoid Kratom

On September 11, 2018, FDA Commissioner Scott Gottlieb, M.D., urged consumers not to use products containing the kratom, an herb that is often promoted for pain relief and for relieving symptoms of opioid withdrawal.

April 03, 2018

FDA Issues Mandatory Recall of Salmonella-Contaminated Kratom Products

On April 2, 2018, the FDA issued a mandatory recall of all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC because several of company's products were found to be contaminated with Salmonella.

April 02, 2018

NutriZone Kratom Supplements Recalled Due to Salmonella Risk

On March 10, 2018, NutriZone, LLC issued a recall of certain kratom-containing powder products because they have the potential to be contaminated with Salmonella.

August 16, 2018

Kratom Recalled Due to Salmonella Risk

On August 14, 2018, Zakah Life, LLC issued a recall of Super Green Maeng Da Premium Kratom powder, Powerful Red Vein Bali Premium Kratom powder, Super Green Maeng Da Premium Kratom capsules, and Powerful Red Vein Bali Premium Kratom capsules because laboratory testing revealed the presence of ...

February 22, 2018

Kratom Supplements Recalled and Destroyed

On February 21, 2018, the FDA announced the voluntary destruction and recall of Botany Bay, Enhance Your Life and Divinity kratom supplements. All of the products were manufactured and distributed nationwide by Divinity Products Distribution, located in Grain Valley, Missouri.

February 20, 2018

Salmonella Outbreak Linked to Kratom Powders, Pills and Teas

On February 20, 2018, the Center for Disease Control (CDC) warned consumers not to use kratom in any form because it could be contaminated with Salmonella. The CDC is currently investigating an outbreak of illness caused by Salmonella infection associated with the use of kratom.

October 18, 2017

Total Body Nutrition Warned for Banned Stimulant in Supplements

On September 28, 2017, the FDA issued a warning letter to Total Body Nutrition following a facility inspection which found some of the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

May 26, 2017

"Allergy" Supplement Containing Ephedra Recalled

On February 7, 2017, MusclMasster, LLC (DBA The Green Herb) of Wheat Ridge, CO issued a recall of all bottles of Al-Er-G Capsules , a product promoted to help allergies, because they contain ephedra.

October 04, 2017

Police Officer Dies From Kratom Overdose, Herb Currently Legal in Most States

A police officer who worked in narcotics in Tupper Lake, New York, died this summer of an overdose of the herb kratom, according to a report from ABC News.

July 29, 2017

Increase in Calls to Poison Control Centers About Supplements

The number of calls to poison control centers in the U.S. about dietary supplement exposures increased by almost 50% between 2005 and 2012, according to a study published this week in the Journal of Medical Toxicology.

January 28, 2017

FDA Testing Confirms Elevated Levels of Belladonna in Some Homeopathic Teething Products

On January 27, 2017, the FDA announced that its laboratory analysis found "inconsistent amounts of belladonna, a toxic substance, in certain homeopathic teething tablets, sometimes far exceeding the amount claimed on the label.

April 15, 2017

Hyland's Baby Teething Tablets and Nighttime Teething Tablets Recalled

On April 13, 2017, Standard Homeopathic Company its Hyland's Baby Teething Tablets and Hyland's Baby Nighttime Teething Tablets because FDA testing has found the tablets contain inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the ...

February 09, 2017

Herbal Supplement Found to Contain Ephedra Alkaloids Recalled

On February 7, 2017, Kingsway Trading Inc. issued a recall of Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement because it contains ephedra alkaloids.

August 31, 2016

Seller of Joint Supplement Warned for Manufacturing Violations, Drug Claims

On July 15, 2016, the FDA issued a warning letter to Vitalife Inc.

August 23, 2016

Seller of Aloe Liquid and Capsules Warned for Manufacturing Violations, Drug Claims

On July 15, 2016, the FDA issued a warning letter to Aloe Farms, Inc.

September 14, 2016

Seller of Aloe, Prostate and Joint Supplements Warned for Manufacturing Violations

On April 8, 2016, the FDA issued a warning letter to Salud Natural Entrepreneurs, Inc.

September 07, 2016

Seller of Herbal Formulas for Cholesterol, Prostate & More Warned For Drug Claims

On July 29, 2016, the FDA issued a warning letter to Healing-Scents following a review of the company's website, which found statements made about its products, Heart Herbs, Cholesterol Regulation Herbs, Diabetes Regulation Herbs, Prostate Healer Herbs, High Blood Pressure Herbs, ...

September 06, 2016

Seller on Noni Juice Warned for Manufacturing Violations, Drug Claims

On August 26, 2016, the FDA issued a warning letter to Healing Noni Co. L.L.C.

November 25, 2016

Homeopathic Teething Tablets and Ear Relief Products Containing Belladonna Recalled

On November 24, 2016, Raritan Pharmaceuticals, a contract manufacturer for Homeolab USA, issued a recall of three homeopathic products for infants and/or children which contain belladonna extract. The products may contain belladonna alkaloids, compounds which can have harmful effects in people.

October 25, 2016

FDA Warns Maker of Sublingual Melatonin and Progesterone Cream

On October 12, 2016, the FDA issued a warning letter to Threshold Enterprises, Ltd.

October 18, 2016

Seller of Sublingual Vitamins Warned for Drug Claims

On August 31, 2016, the FDA issued a warning letter to Bio-Stasis International, Inc., following a review of the company's website which found statements made about its sublingual tablets, ViraPress, Vitamin D-3 and Vitamin B-12. to be drug claims.

December 08, 2017

Limbrel Capsules for Osteoarthritis Linked With Potentially Life-Threatening Health Risk, FDA Warns

On December 4, 2017, the FDA urged consumers not to take Limbrel (Primus Pharmaceuticals), a capsule marketed to manage the metabolic processes associated with osteoarthritis, because it has been associated with serious adverse events, including drug-induced liver injury and a lung ...

November 14, 2017

36 Deaths Associated With the Use of Kratom Products

On November 14, 2017, FDA Commissioner Scott Gottlieb, M.D. issued a statement on the dangers of using products containing kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms.

August 02, 2016

Seller of Whey Protein Warned for Manufacturing Violations, Drug Claims

On July 22, 2016, the FDA issued a warning letter to New Horizon Nutraceuticals, LLC, following a facility inspection which found the company's product, One World Whey Protein Power Food to be adulterated because it was prepared, packed, or held under conditions that violate Current ...

May 24, 2016

Seller of Joint Health, Omega-3 Supplements & More Warned for Manufacturing Violations, Drug Claims

On May 13, 2016, the FDA issued a warning letter to Rocky Fork Formulas, Inc.

May 15, 2016

Seller of Vision Supplements Warned for Drug Claims

On April 28, 2016, the FDA issued a warning letter to Macular Health, LLC.

January 20, 2016

Maker of Growth Hormone, Testosterone Booster Warned for Manufacturing Violations, Misbranding

On January 8, 2016, the FDA issued a warning letter to Nutraloid Labs Inc.

January 20, 2016

Seller of Aloe, Moringa Supplements Warned for Manufacturing Violations, Drug Claims

On January 13, 2016, the FDA issued a warning letter to Alkebulan International Services, LLC, following a facility inspection which found the company's products,Aloe Ferox and Moringa Oleifera Capsule to be adulterated because they prepared, packed, or held under conditions that ...

January 16, 2016

Seller of Liver, Lung Support Supplements Warned for Drug Claims

On January 4, 2016, the FDA issued a warning letter to Tibetan Herbal Balance, Inc.

January 26, 2016

Seller of CoQ10, SAM-e, Vitamin D, and More Warned for Manufacturing Violations, Drug Claims

On January 15, 2016, the FDA issued a warning letter to Nutri-Dyn Midwest, Inc., following a facility inspection which found the company's products, including Cardioauxin BP, Zinc Lozenge, Oliver, Pau D'Arco, Petadolex, Chondro Jointaide, Dynagesic, SAMe-200, Gugulipid.

February 06, 2016

Seller of Turmeric, Milk Thistle and More Warned for Manufacturing Violations, Drug Claims

On January 15, 2016, the FDA issued a warning letter to Terra Firma Botanicals, Inc.

October 21, 2015

Imported Supplements Can Be Dangerous, FDA Warns

On October 15, 2015, the FDA warned consumers that some supplements sold at nontraditional places, such as ethnic or international stores, flea markets, swap meets, as well as online, are often imported from other countries, and some can potentially be harmful.

November 18, 2015

Seller of "Hangover" Supplement Warned for Manufacturing Violations & Drug Claims

On September 17, 2015, the FDA issued a warning letter to Life Support Development Ltd, following a facility inspection which found the company's product, including Life Support Hangover Relief to be adulterated because they prepared, packed, or held under conditions that violate ...

December 29, 2015

Maker of Vitamin K, Vitamin A & More Warned for Manufacturing Violations, Drug Claims

On December 10 2015, the FDA issued a warning letter to Dherbs Health Emporium, Inc.

July 02, 2015

Maker of Arthritis Supplement Warned for Manufacturing Violations, Drug Claims

On June 17, 2015, the FDA issued a warning letter to Desert Stream, Inc.

August 06, 2015

Children and Adult Gummy Vitamins Recalled in Canada Due to Excessive Vitamin D

On August 6, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced Church & Dwight Canada Corp. is recalling the following supplements because they contain more vitamin D than claimed on the label (identified in Canada by their assigned natural product number (NPN):

September 05, 2015

Maker of Multivitamin and Fish Oil Warned for Manufacturing Violations

On July 22, 2015, the FDA issued a warning letter to Westar Nutritional Corp. dba Viva Life Science, Inc.

October 14, 2015

No Vinpocetine in Some Vinpocetine Supplements; Picamilon Labels Not Accurate

A recently published study of 23 supplements listing vinpocetine as an ingredient found six did not contain any vinpocetine. Among those that did contain vinpocetine, most did not list amounts on the label, but amounts found in suggested daily servings varied by almost 100-fold, from 0.

September 26, 2015

Seller of Muscle Supplements and More Warned for Manufacturing Violations

On August 14, 2015, the FDA issued a warning letter to Chaotic Labz, Inc.

February 13, 2014

Maker of Cholesterol and Workout Supplements Warned For Manufacturing Violations, Drug Claims and Unapproved Ingredient

On January 31, 2014, the FDA issued a warning letter to Exclusive Supplements Inc.

December 24, 2013

Muscle Growth Supplement Linked with Liver Failure

On December 23, 2013, the FDA advised consumers to immediately stop using muscle growth supplement Mass Destruction (by Blunt Force Nutrition) because it is labeled as containing at least one synthetic anabolic steroid and has been linked to at least one reported case of liver failure.

October 09, 2013

FDA Warns Consumers Not to Use OxyElite Pro As It Investigates Link With Hepatitis

On October 8, 2013, the FDA warned consumers not to buy or use USPLabs’ weight loss supplement OxyElite Pro because it has been linked with 24 cases of acute non-viral hepatitis in Hawaii.

October 30, 2013

Three Sexual Enhancement Supplements Found to Contain Prescription Drugs

On September 24, 2013, the FDA advised consumers not to purchase or use sexual enhancement supplements Xzen 1200, Xzen Gold and Xzen Xpress because they have been found to contain undeclared prescription drugs.

July 28, 2013

B Vitamin Supplement Found To Contain Anabolic Steroids

On July 26, 2013, the FDA warned consumers not to purchase or use Healthy Life Chemistry by Purity First B-50, a vitamin B dietary supplement which was found to contain anabolic steroids, methasterone and dimethazine.

September 15, 2013

Creatine Powder Containing DMAA Recalled

On September 12, 2013, Ge Pharma, LLC issued a recall of grape and fruit punch flavors of Creafuse Powder because they contain 1,3 dimethylamylamine (DMAA).

January 31, 2015

Maker of Soy and Zinc Warned for Manufacturing Violations

On December 18, 2014, the FDA issued a warning letter to PreMark Health Science, Inc.

February 10, 2015

Seller of "Natural" Cough Syrup Warned for Manufacturing Violations, Drug Claims

On January 21, 2015, the FDA issued a warning letter to Fragrance Manufacturing Incorporated, following a facility inspection which found the company's products, including Maty's All Natural Cough Syrup and Maty's All Natural Cough Syrup for Kids, to be adulterated because they ...

February 24, 2015

Seller of Heart, Brain and Diabetes Supplements Warned for Drug Claims

On February 6, 2015, the FDA issued a warning letter to LCW, Inc.

January 27, 2015

Seller of Aloe, Sexual Enhancement Supplements and More Warned for Manufacturing Violations, Drug Claims

On January 8, 2015, the FDA issued a warning letter to Aloe Man, Inc., following a facility inspection which found the company's products, including The Aloe Man's Super Bright, Dr. Johnson's Maximum Desire, Dr. Johnson's Body Healer, and Dr.

January 16, 2015

CVS Sued for Eye Health Supplement Claims

A class-action lawsuit has been filed against CVS for promoting the company's Advanced Eye Health supplement as comparable to the formula used in the large National Institutes of Health (NIH) eye disease study known as AREDS2, despite the fact that it does not contain the same ingredients.

November 11, 2014

Seller of Sexual, Muscle Enhancement Supplements Warned for Manufacturing Violations and Drug Claims

On August 26, 2014, the FDA issued a warning letter to GE Pharma LLC following a facility inspection which found the company's products, including Fire Burn, Fire Storm, Creatine, Amino Fire, Nitric Fire, Jet Fire, Oxy Fire, HGH, Cissus, Hydro shield, Performa-Test, Raspberry Ketones, Fire Drol, ...

June 17, 2015

Maker of Joint Supplement Warned for Manufacturing Violations

On May 29, 2015, the FDA issued a warning letter to Total Health Advanced Nutrition, Inc.

June 03, 2015

Maker of B-12 Energy Supplement Warned for Manufacturing Violations

On May 15, 2015, the FDA issued a warning letter to LiquidCapsule Manufacturing, LLC.

May 30, 2015

Seller of Supplements for Herpes, Prostate Cancer & More Warned for Drug Claims

On May 7, 2015, the FDA issued a warning letter to Strictly Health Corporation, following a review of the company's websites which found statements made about FENVIR, Prosta Pep and Tonalin brand CLA to be drug claims.

May 23, 2015

Seller of Magnesium, Calcium, Silver and More Warned for Manufacturing Violations, Drug Claims

On May 8, 2015, the FDA issued a warning letter to Pick and Pay, Inc.

May 02, 2015

Maker of Garcinia, Joint Supplements and More Warned for Manufacturing Violations, Drug Claims

On March 25, 2015, the FDA issued a warning letter to JW Nutritional LLC, following a facility inspection which found the company's products, including  Vanish V2 Domestic, Mr.

March 10, 2015

Seller of Vision Supplements Warned for Manufacturing Violations, Drug Claims

On February 26, 2015, the FDA issued a warning letter to Biosyntrx, following a facility inspection which found the company's products, including BioTears Oral Gel Caps, ZoOmega-3 Concentrated Pharmaceutical-Grade Fish Oil, EpiCor A Nutrient-dense High Metabolite Immunogen, Sight C+ Mineral ...

February 28, 2015

Drugs Found in Male Enhancement Supplements

On December 11, 2014, the FDA issued a warning letter to Biogenix USA, LLC, following a facility inspection which found the company's sexual enhancement products, HAM, CE6 and SARMZ to contain undeclared drugs, as well as drugs which were listed on the label but are not permitted ...

May 03, 2010

FDA Warns Consumers to Avoid Breath Supplement Contaminated with Lead

On May 3, 2010 the U.S. Food and Drug Administration warned consumers not to purchase nor consume Vita Breath, a dietary supplement manufactured by American Herbal Lab Inc. of Rosemead, Calif.

December 17, 2010

FDA Steps Up Efforts to Battle Tainted Supplements

On Dec. 15, 2010, the Food and Drug Administration (FDA) took new steps aimed at keeping consumers safe from harmful products that are marketed as dietary supplements and that contain undeclared or deceptively labeled ingredients.

February 07, 2011

Maker of Hoodia and Green Tea Products to Pay $2.65 Million Settlement for Unfair Business Practices

On February 1, 2011, supplement maker Irwin Naturals agreed to pay civil penalties, consumer restitution, and and investigative costs to settle a suit in California alleging that Irwin Naturals marketed Hoodia products that did not contain the hoodia gordonii herb despite the product labeling.

August 07, 2011

Performance Enhancing Ingredient, DMAA, Not Really from Geraniums, Putting Its Use in Supplements in Doubt

On July 29, 2011, the American Herbal Products Association (AHPA) announced a new requirement that products containing the sports performance enhancing compound DMAA (also known as 1,3-dimethlypentlyamine, 1,3 dimethylamylamine, methylhexanamine, or MHA), not be labeled as geranium oil or any part ...

July 19, 2011

FDA Warns of Unsafe Drug in Slimming Supplements

On July 8, 2011, the U.S. FDA advised consumers not to purchase or use Slim Forte Slimming Capsule and Slim Forte Double Power Slimming Capsules. FDA laboratory analysis confirmed that these products contain sibutramine. Sibutramine is a controlled substance that was removed from the U.S.

June 18, 2011

FTC Attacks Massive Online Fraud Regarding "Free Trials" of Supplements and Health Products

On May 17, 2011, the U.S. Federal Trade Commission (FTC) announced that it is suing the operators of an online operation that collected more than $450 million from consumers in the United States, Canada, the United Kingdom, Australia, and New Zealand. According to the FTC's complaint:

April 16, 2012

Protein Supplement Maker Fails FDA Audit -- Many Products Affected

The FDA sent a Warning Letter (dated April 2, 2012) to Theta Brothers Sports Nutrition, Inc. regarding numerous violations of good manufacturing practices at its Lakewood, New Jersey facility.

November 06, 2012

Recall of "Bee Pollen" Supplement Found to Contain Drug

On October 24, 2012, Zi Xiu Tang Success, LLC issued a voluntary recall of Classic Zi Xiu Tang Bee Pollen Capsules and Ultimate Formula Capsules because the supplements contain the undeclared drug sibutramine.

May 17, 2013

Hoodia, Sexual Enhancement Supplements and More Found To Be Adulterated, Misbranded

On March 01, 2013, the FDA issued a warning letter to Desert Rose Manufacturing, Inc.

January 30, 2013

Maker of Cold and Flu Supplement Warned For Making Drug Claims

On January 24, 2013, the FDA and FTC jointly issued a warning letter to Flu and Cold Defense LLC, after a review of the company's website and marketing materials found statements made about the cold and flu dietary supplement GermBullet to be drug claims.

January 24, 2013

Excessive Lead and Mercury Found In Chinese Herbal Supplements

On January 23, 2013, Health Canada warned consumers that certain batches of the Chinese dietary supplements [W.S.

February 12, 2013

Judge Orders Drug and Supplement Company to Cease Manufacturing and Distribution

On February 8, 2012, the FDA announced Titan Medical Enterprises Inc. has been ordered to stop manufacturing and distributing drugs and dietary supplements until the company's manufacturing operations comply with the Federal Food, Drug, and Cosmetic Act. The order was signed on December 11, 2012, U.

July 24, 2006

Marketers of Seasilver Ordered to Pay Almost $120 Million

On July 24, 2006, the Federal Trade Commission (FTC) announced that the marketers of Seasilver, an alleged phony cure-all, have been ordered to pay almost $120 million for failing to comply with an earlier order requiring them to pay $3 million in consumer redress.

December 02, 2005

Steroids Detected In Supplement

On November 30, 2005, The Washington Post reported that a dietary supplement marketed to fitness and health enthusiasts on the Internet and in body-building shops contains anabolic steroids, according to a prominent researcher.

April 22, 2008

Court Upholds Order for Seasilver Marketers to Pay $120 Million

On April 16, 2008, the Federal Trade Commission (FTC) announced that the U.S.

November 28, 2006

FTC Targets Seller of Pills Promoted for Height, Weight, and Bone Improvement

On November 28, 2006, the Federal Trade Commission (FTC) announced that a Florida business and its owner, who marketed purported height-enhancing pills for kids and young adults, will pay $375,000 to settle charges that their advertising claims were deceptive.

January 18, 2024

FDA Warns Consumers Not to Use Neptune’s Fix Products

On November 21, 2023, the FDA warned consumers not to purchase or use Neptune’s Fix products because they contain tianeptine. The FDA has received severe adverse event reports after use of these products, including seizure and loss of consciousness.

February 20, 2024

Nordic Naturals Infant Liquid Vitamin D Recalled Due to Excessive Vitamin D

On February 17, 2024, Nordic Naturals issued a recall of one lot (approximately 3,800 units) of Nordic Naturals Baby’s Vitamin D3 Liquid because it contains elevated levels of vitamin D. The product is labeled as containing 400 IU (10 mcg) per the suggested serving of 0.25 mL.

March 10, 2018

Kratom Supplements Recalled Due to Salmonella Risk

On March 10, 2018, PDX Aromatics of Portland, Oregon DBA Kraken Kratom, Phytoextractum, and Soul Speciosa issued a recall of certain kratom-containing powder products because they have the potential to be contaminated with Salmonella.

June 23, 2018

Gaia Kratom Recalled Due to Salmonella Risk

On June 21, 2018, Gaia Ethnobotanical, LLC issued a recall of 27 kratom products because they have the potential to be contaminated with Salmonella.

January 12, 2021

FDA Warns Seller of Joint and Hair Loss Products

On December 22, 2020, the FDA issued a warning letter to Speedwinds Nutrition, Inc. following a review of the company's website, which found statements made about the company's products Synotrex and Sephren to be drug claims.

March 30, 2021

Real Water Alkaline Water Recalled for Possible Link to Liver Illness

On March 24, 2021, Real Water, Inc. recalled all sizes of Real Water bottled alkaline water because it may be linked to multiple cases of non-viral hepatitis that occurred in Las Vegas, NV in November of 2020.

August 28, 2023

Dr. Berne’s MSM and Castor Oil Eye Drops Recalled Due to Bacterial and Fungal Contamination

On August 26, 2023, Dr. Berne’s Whole Health Products issued a recall of all lots of its MSM DROPS 5%, 15% Solution, Dr. Berne’s Organic Castor Oil Eye Drops and Dr. Berne’s MSM MIST 15% Solution due to the risk of bacterial and fungal contamination.

June 14, 2007

Marketers of Bogus Growth Hormone Sprays Settle with FTC

On May 29, 2007 the Federal Trade Commission (FTC)announced that two operations that marketed oral sprays that were supposed to help users lose weight, reverse the aging process, and prevent or treat diseases have settled FTC charges that their claims were bogus.

September 25, 2007

Recall of Contaminated Baby Supplement

On September 21, 2007 the U.S. Food and Drug Administration (FDA) warned consumers not to consume Baby's Bliss Gripe Water, apple flavor, with a code of 26952V and expiration date of October 2008 (shown as '10/08' on the label). The product is distributed by MOM Enterprises, Inc.

October 18, 2005

FTC Stops False Claims about HGH Oral Spray

On October 18, 2005, the Federal Trade Commission (FTC) announced that, at its request, a federal court issued a temporary restraining order against marketers of oral sprays that supposedly contain human growth hormone (HGH) to stop them from making alleged false and deceptive claims and from ...

February 15, 2006

New Zealand Warns of Liver Toxicity from Black Cohosh

On February 9, 2006, New Zealand's Therapeutic Goods Administration (TGA) announced new labelling and consumer information for medicines containing Black cohosh (Cimicifuga racemosa).

July 30, 2004

FTC Sues Florida Man for Illegal Spam and False "Human Growth Hormone" Product Claims

On July 29, 2004, The Federal Trade Commission (FTC) reported that a federal court in Chicago has issued a court order halting illegal spamming and deceptive product claims, and has also frozen the assets of Creaghan A. Harry, a resident of Boca Raton, Florida.

March 11, 2003

Rexall Agrees to Pay up to $12 million to Users of Misleading Cellulite Supplement

On March 11, 2003, the Federal Trade Commission (FTC) reported that Rexall Sundown, Inc. (Rexall) will pay up to $12 million to resolve FTC charges regarding its marketing of the dietary supplement, "Cellasene," a purported cellulite treatment product.

January 03, 2004

FDA to Prohibit Sales of Dietary Supplements Containing Ephedra

On December 30, 2003, the U.S. Food and Drug Administration (FDA) issued a consumer alert of its forthcoming determination that dietary supplements containing ephedra present an unreasonable risk of illness or injury, and should not be consumed.

February 21, 2013

FDA and FTC Warn: Supplements Cannot Prevent, Treat Or Cure Cold And Flu

On February 11, 2013, the FDA and the Federal Trade Commission (FTC) jointly issued warning letters to three dietary supplement companies regarding their potential illegal marketing of products to prevent, treat or cure flu virus.

March 29, 2013

Prescription Drugs Found In Prostate and Sexual Enhancement Supplements

October 24, 2012 the FDA issued a warning letter to USA Far Ocean Group Inc./ Health & Beauty Group Inc. because a number of the company's dietary supplements were found to contain pharmaceutical drugs, or were promoted with statements that constitute drug claims.

October 24, 2012

FDA Seizes Many Supplements from New York Company Due To Drug Claims

On October 23, 2012, U.S. Marshalls, acting on behalf of the FDA, seized dietary supplements and unapproved drugs from Confidence, Inc., a supplement manufacturer in Port Washington, N.Y. The products included dietary supplements Dr.

January 10, 2012

Acai Berry Pill Marketers to Pay $1.5 Million to Settle FTC Charges

On January 9, 2012, the U.S. Federal Trade Commission (FTC) announced that an operation that marketed acai berry supplements, "colon cleansers," and other products using allegedly fraudulent free trial offers and phony endorsements from Oprah Winfrey and Rachael Ray will pay $1.

August 31, 2009

Court Orders Marketers of Supreme Greens and Coral Calcium to Pay Nearly $70 Million for Consumer Refunds

On August 27, 2009, a federal district court ordered the marketers of two dietary supplements – "Supreme Greens" and "Coral Calcium" – who claimed the products would cure ailments ranging from cancer and Parkinson’s disease to heart disease and autoimmune diseases to pay nearly $70 million for ...

May 01, 2009

FDA Warns Consumers to Stop Using Hydroxycut -- Product Being Tested by ConsumerLab.com

On May 1, 2009, the U.S. Food and Drug Administration warned consumers to immediately stop using Hydroxycut products by Iovate Health Sciences Inc., of Oakville, Ontario and distributed by Iovate Health Sciences USA Inc. of Blasdell, N.Y.

March 10, 2015

Maker of Magnesium, Calcium, Zinc, B Vitamins and More Warned for Manufacturing Violations, Drug Claims

On January 8, 2015, the FDA issued a warning letter to Complete H2O Minerals, following a facility inspection which found the company's products, including Sulfur Concentrate, Copper, Extra Strength Copper, Extra Strength Magnesium, Extra Strength Zinc, Platinum, Gold, Indium, Molybdenum, ...

May 30, 2015

Seller of Omega-3, Probiotics & SuperFoods Warned for Manufacturing Violations, Drug Claims

On May 4, 2015, the FDA issued a warning letter to Dr. Dennis Black, LLC.

June 11, 2015

FDA Warns Maker of Fruit Energy Drinks for Drug Claims

On May 19, 2015, the FDA issued a warning letter to CK Management, Inc. following a facility inspection which found statements made on product labels and websites about Whole5, Fruit of the Spirit and ViaViente "whole food" fruit puree energy drinks to be drug claims.

February 24, 2015

Seller of Antioxidant Water, Energy Drops Warned for Manufacturing Violations and Drug Claims

On February 18, 2015, the FDA issued a warning letter to Better Health Lab, Inc.

August 02, 2013

Vitamin B, Vitamin C and Multimineral Supplements Recalled Due To Anabolic Steroid Risk

On July 31, 2013, Purity First Health Products, Inc.

June 26, 2015

Seller of CoQ10, Anxiety Supplements and More Warned for Manufacturing Violations, Drug Claims

On June 6, 2015, the FDA issued a warning letter to Country Doctor Herbals, following a facility inspection which found the company's products, including  Herbal Flu Be-Gone, Herbal Multi-Bac, Herbal Nervine, Herbal Pain-A-Way, Herbal Pancreas, Herbal Parasite Cleanse, Herbal Perfect ...

December 16, 2015

Maker of Red Yeast Rice, St. John's Wort, Valerian and More Warned for Manufacturing Violations, Drug Claims

On December 2, 2015, the FDA issued a warning letter to Nature's Health, LLC, following a facility inspection which found the company's product, including Ginkgo & Rhodiola, Blood Sugar Balance IV, Cinnamon Extract, Choles-Balance Red Yeast Extract, Lecithin, Milk Thistle Seed Extract, ...

November 07, 2015

Seller of "NaturalDoctor" Vitamin C, Echinacea and More Warned for Manufacturing Violations

On October 16, 2015, the FDA issued a warning letter Sound Healing Arts, PC, dba Grounds for Tea, LLC, following a facility inspection which found the company's products, including  NaturalDoctor Vitamins C & K3, NaturalDoctor Goldenseal & Echinacea Plus, NaturalDoctor Centella ...

November 04, 2016

Liver Injuries Linked With Dietary Supplement Use on the Rise

The number of liver injuries associated with dietary supplement use has increased substantially in recent years, according to a recently published study in the journal Hepatology.

June 26, 2024

FDA Warns Consumers Not to Use Infla-650 Due to Undeclared Drugs

On June 20, 2024, the FDA warned consumers not to purchase or use Infla-650 after FDA laboratory analysis found them to contain acetaminophen, diclofenac, and phenylbutazone.

July 16, 2024

Infla-650 Herbal Dietary Supplement Recalled

On July 16, 2024, Guru Inc. issued a recall of one lot of Infla-650 Herbal Dietary Capsules because they were found to contain acetaminophen, diclofenac, and phenylbutazone.

February 28, 2024

Microbial Contamination Found in LightEyez MSM Eye Drops

On February 15, 2024, the FDA issued a Warning Letter to LightEyez Limited after testing by the agency found the company’s LightEyez.com MSM Eye Drops V2.0 — Eye Repair (MSM Eye Repair Drops) to have microbial contamination in samples of the drops.

January 15, 2024

Suprex Carb & Sugar Block Recalled

On December 7, 2023, Vita 360, LLC issued a recall of one lot of SUPREX Plant Based Nutrition Carb & Sugar Block after FDA analysis found it to contain only 16 mcg of chromium per serving and not 100 mcg of chromium per serving, as listed on the label.

May 01, 2024

FDA Warns Consumers Not to Use Ossos-Sans Supplement for Joints

On April 17, 2024, the FDA warned consumers not to purchase or use Ossos-Sans, a supplement promoted to treat osteoarthritis, osteoporosis, and other conditions, because it contains undeclared drugs, including diclofenac and methocarbamol.

March 18, 2021

Don't Drink Real Water Alkaline Water, FDA Warns After Reports of Liver Illness

On March 16, 2021, the FDA warned consumers not to drink or use Real Water bottled alkaline water while it investigates reports of hepatitis associated with the product.

July 06, 2022

Two Companies Banned From Selling Supplements to Treat Heart Disease, Neuropathy

On June 30, 2022, the Federal Trade Commission (FTC) finalized an administrative complaint order against two Texas-based companies, Health Research Laboratories, LLC and Whole Body Supplements, LLC, for making unverified claims that their products can prevent or treat disease.

July 22, 2024

Umary Hyaluronic Acid Supplement Recalled

On July 15, 2024, SoloVital.

April 25, 2024

Drug Found in Umary Supplement

On April 18, 2024, CTV News in Canada reported tests suggesting that Umary Hyaluronic Acid Dietary Supplement may be adulterated with the prescription anti-inflammatory drug diclofenac, which may explain side effects that have been reported with its use.

May 28, 2003

FTC Challenges Claims of Five Supplements to Treat or Cure Serious Diseases

On May 27, 2003 the Federal Trade Commission announced that it had filed a complaint in federal district court against A.

August 03, 2023

Arsenic Poisoning in U.S. from Ayurvedic Supplements

A 75-year-old woman in California experienced arsenic poisoning after taking Ayurvedic supplements prescribed to her by a holistic energy healer, according to a report published in July in Clinical Case Reports.

September 25, 2023

FDA Warns Consumers Not to Use Tapee Tea

On August 31, 2023, the FDA warned consumers not to purchase or use Tapee Tea products after FDA laboratory analysis found them to contain dexamethasone and piroxicam, drugs that are not listed on the product's label.

November 29, 2023

Dr. Berne’s Whole Health Products Warned for Contaminated Eye Drop Products, Drug Claims

On November 22, 2023, the FDA issued a Warning Letter to Dr. Berne’s Whole Health Products following review of the company’s website, which found statements about the company’s Dr. Berne’s MSM Eye Drops 5%, Dr. Berne’s MSM Eye Drops 15%, and Dr.

December 07, 2023

Belmont Eyecare Warned for Colloidal Silver, MSM, and Castor Oil Eye Drop Claims

On December 1, 2023, the FDA issued a Warning Letter to Belmont Eyecare LLC, following a review of the company’s website, which found statements about the company’s Colloidal Silver Eye Drops, MSM Eye Drops, Organic Daytime Oil Eye Drops, Organic Daytime Oil Eye Drops Small, Organic ...

December 14, 2023

Pain Relief Tea Recalled, Found to Contain Prescription Drugs

On December 13, 2023, WS Global issued a recall of all lots of the company’s Himalayan Pain Relief Tea after products were found to contain diclofenac and dexamethasone, prescription drugs that are not listed on the product’s label.

February 22, 2021

Canadian Creatine Recalled for Dangerous Levels of Vitamin D

On February 21, 2021, the Canadian company Genex Nutraceuticals recalled one lot of Perfect Sports Core Series Pure Creatine (also known as Creatine Powder) because it "contains vitamin D that is not listed on the label, at dangerous levels.

September 06, 2022

Sand Ginger Powder Recalled in Canada Due to Aconite

On September 1, 2022, Ka Wing Hong issued a recall of Mr. Right brand Keampferia Galanga Powder (sand ginger powder), a common spice used in Asian cuisine, due to aconitine contamination.

July 25, 2022

Nature’s Sunshine Protein Powder Recalled

On July 22, 2022, Nature’s Sunshine Products Inc. issued a recall of two AIVIA Whey Protein Powder Herbs meal replacement products due to undeclared milk.

March 09, 2022

FDA Warns Seller of Magnesium, CBD, Herbal Extracts & More

On February 9, 2022, the FDA issued a warning letter to Bea Lydecker’s Naturals, Inc.

January 18, 2005

Supplement Maker to Pay over $3.5 Million to Settle Deceptive Advertising Charges for Immune Dietary Supplement

On January 18, 2005, the Federal Trade Commission (FTC), the Orange County (California) District Attorney, and the California State Attorney General announced that they had reached settlements with Body Wise International, Inc.

July 15, 2019

Mislabeled Green Tea Supplement Recalled

On July 11, 2019, DaVinci Laboratories of Vermont issued a recall of 256 bottles of the weight management supplement Dim Plex because they may undeclared fish allergens. 

April 17, 2020

Seller of Vitamin D, MSM, Selenium & More Warned for Drug Claims

On March 31, 2020, the FDA issued a warning letter to KetoKerri LLC following a review of the company's website, which found statements made about some of the company's products, including Dr.

December 29, 2020

FDA Warns Five Sellers of CBD for Claims of Treating Arthritis, Alzheimer's and More

On December 22, 2020, the FDA issued warning letters to five sellers of CBD following reviews of the companies' websites, which found statements made about the companies' products to be drug claims.

March 04, 2021

Federal Court Bars Confidence USA from Selling Supplements

On March 4, 2021, the FDA announced a permanent injunction has been entered, barring dietary supplement manufacturer Confidence USA Inc. and two of its executives from producing or selling products until they become compliant with current good manufacturing practices (cGMPs).

July 21, 2003

FTC Stops False Advertising of Heavily Promoted Supplements for Breast Enhancment, Male Virility, and Snoring

On June 10, 2003, the Federal Trade Commission (FTC) announced that infomercial marketers Wellquest International, Inc. and Tony Hoffman Productions, Inc.

June 16, 2009

FDA Warns of Loss of Sense of Smell with Zicam Nasal Gel/Nasal Swab

On June 16, 2009, the U.S. FDA warned consumers and healthcare professionals to discontinue use of three Zicam Nasal Gel/Nasal Swab products sold over-the-counter as cold remedies because they are associated with the loss of sense of smell that may be long-lasting or permanent.

February 09, 2019

Herbal Skin Remedy Recalled, Can Cause Serious Injury

On February 8, 2019, McDaniel Life-Line LLC issued a recall of all lots of Indian Herb a product marketed to be taken orally or applied topically, as a remedy for abnormal skin growths.

December 21, 2019

Supplement Company Continues to Make False Claims About Its Products, Says FTC

The FTC has filed a motion of contempt against two supplement companies that, according to the motion, have continued to promote their products with false claims despite being barred from doing so by a previous court order.

March 20, 2020

Kudzu Supplement Recalled for Salmonella Risk

On March 18, 2020, Mountain Rose Herbs issued a recall of all sizes of Organic Kudzu Root Herbal Supplement because recent testing found it has the potential to be contaminated with Salmonella.

January 04, 2020

Hormonal Balance Supplement Tied to Liver Failure

An otherwise healthy 23-year old woman in Texas is reported to have recently developed liver failure (requiring a liver transplant) after taking the supplement Balance (from Alani Nu) for four months.

December 27, 2019

Federal Court Shuts Down Three Supplement Companies With Serious Manufacturing Violations

Update: (1/23/20) ABH has issued a recall of all its products, which are sold under various brand names by over 800 distributors and retailers. More details are available in CL's post about this recall.

September 18, 2015

High Levels of Mercury and Lead Found in Ayurvedic Herbal Supplements

On September 17, 2015, the FDA announced that Shree Baidyanath Ayurved Bhawan Ayurvedic dietary supplements were found to contain high levels of lead and/or mercury, which can cause serious health problems.

July 15, 2004

Company Stopped by FTC from Claiming to Prevent or Reverse Memory Loss without Evidence

On July 13, 2004, the Federal Trade Commission(FTC) announced that a dietary supplement manufacturer has settled FTC charges that it violated federal law by making unsubstantiated claims that its product, “Senior Moment,” could prevent memory loss and restore memory function in adults.

April 23, 2019

"Brain Boosting" Supplements Were Promoted With Non-Existent Clinical Studies

On April 10th, 2019, the FTC (Federal Trade Commission) announced the marketers of cognitive enhancement supplements Geniux, Xcel, EVO, and Ion-Z have agreed to settle charges that they made false claims about the product, including fake research references and celebrity ...

October 27, 2004

Some Supplements Can Damage Eyes At High Doses and with Topical Use

As reported by Reuters Health on October 21, 2004, an article in the current issue of the American Journal of Ophthalmology suggests that some herbal remedies and nutritional supplements can damage the eyes.

August 25, 2018

Thirty-Two Children's Homeopathic Products Recalled

On August 22, 2018, King Bio issued a recall of 32 homeopathic products for children because some have have tested positive for microbial contamination.

March 28, 2008

FDA Warns of Adverse Reactions with Two Liquid Supplements -- Selenium Toxicity Possible

The U.S. Food and Drug Administration is advising consumers not to purchase or consume Total Body Formula in the flavors of Tropical Orange and Peach Nectar, or Total Body Mega Formula in the Orange/Tangerine flavor.

July 12, 2017

More Bodybuilding Supplements Recalled

On July 11, 2017, Andropharm recalled two bodybuilding supplements, Sten Z and M1 Alpha, because these products contain derivatives of anabolic steroids.

June 20, 2017

Beware of Bodybuilding Supplements, FDA Warns

On June 20, 2017, the FDA warned consumers to beware of bodybuilding products because a number of these products have been found to contain steroids or steroid-like substances. Such products could cause serious and even life-threatening health risks, including: 

April 11, 2008

Update: Hazardous Levels of Selenium Confirmed by FDA in Two Supplements

On April 11, 2008, the FDA notified healthcare professionals and patients that it has found hazardous levels of selenium in samples of certain flavors of the dietary supplement products "Total Body Formula" and "Total Body Mega Formula.

June 03, 2008

Selenium Toxicity from a Supplement

The June 2008 issue of Annals of Internal Medicine provides a recent case report describing the symptoms of a woman and her husband after taking a liquid supplement found to contain excessive selenium.

June 21, 2010

FDA Warns Parents to Be Careful Giving Vitamin D Drops to Infants

On June 15, 2010, the U.S. FDA (Food and Drug Administration) alerted parents and caregivers that some liquid Vitamin D supplement products are sold with droppers that could allow excessive dosing of Vitamin D to infants.

December 13, 2013

Maker of Menopause Blend and Other Supplement Ingredients Warned by FDA of Violations

On November 21, 2013, the FDA issued a warning letter to Raw Deal, Inc.

September 22, 2018

MyoWhey Protein Powder Recalled

On September 20, 2018, Purus Labs, Inc. issued a recall of one lot of MyoWhey Chocolate Cookie Crunch protein powder because it may contain undeclared milk and soy.

April 12, 2013

Zicam Advised Against Using Cold Prevention Claim In Advertising

On April 5, 2013, it was reported that the National Advertising Division (NAD) recommended that Matrixx Initiatives, maker of Zicam cold products, stop making claims in its advertising that the product can prevent colds.

December 19, 2012

Zicam Nasal Gel Recalled Due to Potential Bacterial Contamination

On December 18, 2012, Matrixx Initiatives issued a voluntary recall of a single lot of Zicam Extreme Congestion Relief nasal gel after routine testing confirmed a sample from this lot was contaminated with Burkholderia cepacia.

October 29, 2008

Two Vitamin C Supplements Recalled in Canada for Vitamin A Risk

On October 28, 2008, Health Canada warned Canadians, expecially expectant mothers, not to use two vitamin C products sold under the brand names New Roots Herbal Vitamin C8 and Vitazan Professional Vitamin C Advanced Ascorbate.

December 18, 2006

Canada Warns of Herbal Sleep Product Containing Rx Drug

On December 18, 2006 Health Canada advised consumers not to use a product called Eden Herbal Formulations Sleep Ease Dietary Supplement, because it was found to contain an undeclared drug estazolam, which can be habit-forming when used for as little as a few months.

November 20, 2013

OxyElite Pro Recall Expanded

On November 19, 2013, USPlabs LLC expanded its recall of OxyElite Pro products to include Raspberry Lemonade OxyELITE Pro Super Thermo Powder (4.6 oz., UPC #094922447494).

March 21, 2014

Products Containing Kratom Recalled Following FDA Import Alert

On March 14, 2014, SNI National issued a voluntary recall of all kratom supplements, including kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack, following an FDA-issued import alert on all products containing this ingredient.

April 17, 2015

Herbal Laxative and "Detox" Kit Containing High Levels of Lead and/or Arsenic Recalled in Canada

On April 15, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced that St. Francis Herb Farm Inc.

October 10, 2014

Seller of Multivitamin Warned for Drug Claims

On September 25, 2014, the FDA issued a warning letter to Multimmunity, Inc., following a review of the company's website which found statements made about the dietary supplement Multimmunity to be drug claims.

November 29, 2016

Seller of Mineral, Joint Supplements and More Warned for Manufacturing Violations, Drug Claims

On July 1, 2016, the FDA issued a warning letter to BioGenyx-Basic Reset, following a facility inspection which found the company's products, including Ionyte, Aqualyte, Beta Factor, Bee Gold and Primo Java to be adulterated because they were prepared, packed, or held under ...

July 16, 2016

Herbalife Agrees to Business Restructure and $200 Million Payment to Settle FTC Charges of Deception

Herbalife and its associated companies (Herbalife International America Inc., Herbalife , Ltd.) has agreed to restructure its U.S.

November 04, 2015

Senator Investigates Herbalife Business Practices, Calls for Reforms

A report accusing multi-level-marketing supplement company Herbalife of using "fraudulent practices" and operating an "illegal pyramid scheme" was issued in October of 2015 by New York's Office of State Senator Jeff Klein and Public Advocate Letitia James.

July 01, 2015

Undeclared Drugs Found In Male Enhancement Supplements

On June 10, 2015, the FDA issued a warning letter American Lifestyle, following tests which found the company's sexual enhancement supplements Vicerex and Sudibil-Xr to contain the undeclared drugs propoxyphenyl thioaildenafil and tadalafil.

November 28, 2015

Herbal Supplements Linked to Heavy Metal Poisoning

On November 17, 2015,  Health Canada (the Canadian equivalent of the FDA) warned that a consumer in Canada who purchased and used herbal supplements from a U.S.-based website was treated for heavy metal poisoning.

December 01, 2015

Multivitamins Recalled Due to Risk of Vitamin D Toxicity

On November 25, 2015, Glades Drugs, a compounding pharmacy in Pahokee, Florida, issued a recall of its compounded multivitamin capsules because they contain high amounts of vitamin D3 (exact amount was not reported).

November 04, 2015

Green Tea from Tea Bags Linked to Acute Hepatitis

According to a case report published on September 23, 2015 (Lugg, BMJ Case Rep 2015), a 16-year old girl in England developed acute hepatitis in connection with the consumption of green tea.

March 28, 2017

Yogurt Peanut Crunch Bars Recalled Due to E. Coli Risk

On March 23, 2017, Pro Sports Club of Bellevue, WA issued a recall of 36,957 20/20 Life Styles Yogurt Peanut Crunch bars because they have the potential to be contaminated with Escherichia coli O157:H7.

November 21, 2017

Health Canada Calls for Stronger Warnings of Liver Risk on Green Tea Extract Products

On November 15, 2017, Health Canada (the Canadian equivalent of the FDA) recommended stronger warning statements about the risk of liver toxicity on labels of supplements containing green tea extract sold in Canada. 

December 12, 2014

Seller of B-12, Zinc, Echinacea and More Warned for Manufacturing Violations and Drug Claims

On November 14, 2014, the FDA issued a warning letter to Scientific Botanicals Company, Inc.

November 11, 2013

Workout Supplement OxyElite Pro Recalled After Being Linked to Serious Liver Illness

On November 10, 2013, the FDA announced that USPLabs LLC is recalling workout supplements OxyElite Pro Super Thermo capsules, OxyElite Pro Ultra-Intense Thermo capsules and OxyElite Pro Super Thermo Powder because they have been linked to a number of cases of acute non-viral hepatitis, one of which ...

October 17, 2013

Turmeric Spice Powder Recalled Due To High Lead Levels

On October 3, 2013, the OnTime Distribution Inc. issued a voluntary recall of PRAN brand spice powder Turmeric because it was found to contain high levels of lead.

March 25, 2002

FDA Advises Consumers of Risk of Severe Liver Toxicity with Kava

On March 25, 2002 the U.S. Food and Drug Administration (FDA)issued a Consumer Advisory, as well as a letter to health care providers, advising of the potential risk of severe liver injury associated with the use of kava-containing dietary supplements.

January 31, 2002

Recall Update for Certain Metabolife Bars - Excessive Vitamin A

The U.S. Food and Drug Administration (FDA) released the following Class I recall information in its January 30, 2002 Enforcement Report.

January 02, 2004

Canada Reiterates Warning on Products Containing Kava

On December 23, 2003, Health Canada reminded Canadian consumers of the serious risks associated with the use of products containing kava.

August 31, 2006

Canada Advises Consumers Not To Use Adulterated Sleep Supplement

On August 30, 2006, Health Canada (the Candian Health Ministry) Health Canada advised consumers not to use Salt Spring Herbals Sleep Well Dietary Supplement because a sample analyzed by Health Canada has been found to contain the undeclared drug estazolam, a sedative that can be habit-forming when ...

September 25, 2012

Whey Protein Supplements Recalled Due To Undeclared Allergens

On September 21, 2012, Maine Natural Health, which also sells supplements under the brand name Stronger Faster Healthier, issued a recall of several Whey Protein Concentrate products because the labels do not list the allergens milk, shellfish and coconut.

January 30, 2013

Seller of Omega-3 and Emu Oil Supplements Warned For Drug Claims, Misbranding

On November 19, 2012, the FDA issued a warning letter to Emu Products & Management, Inc. after a review of the company's website found statements that promoted the dietary supplements Multi-Omega Gel Caps, Recovery Gel Caps, ARP Gel Caps and the topical skin products Extreme Cryo Gel, F.A.C.E.

January 31, 2010

Glucomannan May Cause Choking if Not Taken with Fluid

On January 29, 2010, the Canadian health department, Health Canada, adised that natural health products containing the ingredient glucomannan in tablet, capsule or powder form have a potential for harm if taken without at least 8 ounces of water or other fluid.

June 22, 2011

Recall of Calcium & Magnesium Softgels Containing Excessive and Potentially Toxic Amounts of Vitamin D

On or about June 7, 2011, NOW Foods announced the following recall to retailers. ConsumerLab.com was subsequently made aware of the recall by a ConsumerLab.com member.

September 09, 2011

Possible Concern with Fenugreek Based on Contamination in Europe

Products made with fenugreek, including pills containing fenugreek seed, have been pulled from shelves in Germany due to conern over potential contamination with E. coli bacteria. There is no such action in the U.S., but ConsumerLab.

December 20, 2011

Organic Celery Seed Products Recalled Due to Potential Salmonella Contamination

On December 16, 2011, the U.S. FDA posted a notice from Swanson Health Products regarding the recall of Swanson Organic Celery Seed (Whole) which is packaged in plastic bottles with a net weight of 1.4 oz. (40 grams) because it has the potential to be contaminated with Salmonella.

June 04, 2012

FDA Warning on Supplement for Pain Relief

On June 1, 2012, the U.S. FDA warned consumers that Reumofan Plus, marketed as a “natural” dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.