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.

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.

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.

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.

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).

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.

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.

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: 

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.

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.

December 20, 2021

Pantene, Herbal Essences, & Other Brands of Dry Shampoo and Conditioner Recalled Due to Benzene

On December 17, 2021, Procter & Gamble issued a recall of 26 aerosol spray dry shampoos and conditioners from six brands, including Aussie, Herbal Essences, Hair Food, Old Spice, Pantene, and Waterless Hair Care, because some of the products were found to contain benzene.

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.

May 10, 2021

Collagen & Biotin Supplement Recalled Due to Allergen Risk

On May 6, 2021, Bloommy, Inc. issued a recall of Bloommy Biotin Collagen Keratin Capsules for Skin, Joint, and Hair due to the presence of a fish allergen for the collagen-based ingredient.

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.

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.

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.

October 24, 2022

Dove, Suave, Tresemme & Other Dry Shampoos Recalled Due to Benzene

On October 18, 2022, Unilever issued a recall of 19 dry shampoo products including Dove, Suave, and Tresemme after an internal investigation found the products to contain benzene. According to Unilever, the propellants of these products were the source.

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 ...

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

June 16, 2020

FDA Warns Four Companies for Unsafe "Homeopathic" Injectables

On June 16, 2020, the FDA issued warning letters to four manufacturers of unapproved injectable drugs labeled as homeopathic.

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, ...

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.

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

November 09, 2019

Biotin Supplements Can Cause False Lab Test Results

On November 5, 2019, the FDA reminded consumers and health care providers that high amounts of biotin (vitamin B-7), found in many supplements, can significantly interfere with certain lab tests and cause incorrect results that may go undetected.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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. 

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.

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.

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.

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.

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.

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.

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, ...

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:

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.

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:

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:

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:

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.

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:

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.

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 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 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.

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.

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.

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.

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.

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.

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:

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.

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.

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.

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.

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.

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.

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.

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 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.

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 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.

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 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.

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.

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.

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.

July 10, 2017

Bodybuilding Supplements Containing Steroid-Like Substances Recalled

On June 29, 2017, Hardcore Formulations recalled all lots and expiration dates of their products Ultra-Sten and D-Zine, bodybuilding supplements found to contain methylstenbolone and dymethazine, which are derivatives of anabolic steroids.

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:

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.

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.

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.

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.

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.

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, ...

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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

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.

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.

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 ...

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.

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.

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:

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.

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.

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:

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.

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, 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 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.

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, ...

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 ...

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.

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.

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.

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.

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.

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 ...

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.

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.

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.

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."

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.

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.

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.

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.

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.

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.

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.

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.

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).

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.

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.

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.

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.

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).

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.

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.

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 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.

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.

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.

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.

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 ...

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 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).

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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:

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.

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.

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.

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.

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.

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. 

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.

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).

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.

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.

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.

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 ...

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.

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.

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.

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 ...

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.

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.

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.

February 25, 2017

Radio "Infomercials" for Cognitive and Joint Health Supplements Deceived Consumers, Says FTC

On February 22, 2017, the Federal Trade Commission and the Maine Office of the Attorney General announced a complaint the marketers of CogniPrin and FlexiPrin, charging that they made misleading claims about the supplements in radio infomercials deceptively formatted as talk shows.

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 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.

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.

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.

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.

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.

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.

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.

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 ...

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.

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.

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).

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 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.

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.

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 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.

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.

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 ...

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).

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.

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.

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.

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.

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:

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.

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.

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.

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.

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.

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.

May 14, 2014

Maker of Mood, Smoking Cessation Supplements and More Warned for Violations, Drug Claims

On April 17, 2014, the FDA issued a warning letter to CDJ Holding, Incorporated, d.b.a.