Product Reviews and Information for Heart Failure

August 06, 2016

Some Supplements May Cause or Exacerbate Heart Failure (Includes vitamin E and many herbs)

Taking certain supplements may be dangerous for people with heart failure, according to a statement from the American Heart Association (AHA) which was published in the journal Circulation (August 2, 2016). 

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.

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.

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.

October 31, 2017

Black Licorice Can Cause Abnormal Heart Rhythms, FDA Warns

On October 30, 2017, the FDA warned consumers that eating 2 ounces of black licorice a day for at least two weeks could cause an irregular heart rhythm or arrhythmia in adults age 40 or older. 

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.

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.

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.

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.

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.

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 26, 2018

Seller of Coenzyme-A Warned For Making Drug Claims

On January 5, 2018, the FDA issued a warning letter to Coenzyme A, Inc. following a facility inspection and review of the company's website that found the company made drug claims about its product Coenzyme-A.

January 16, 2018

Adverse Effects From Energy Drinks Common Among Youth and Young Adults

More than half (55.4%) of young people who have ever consumed an energy drink have experienced at least one adverse reaction, according to study published yesterday in CMAJ Open, a journal of the Canadian Medical Association.

January 04, 2024

Lone Star Botanicals Warned by FDA for Manufacturing Violations

On November 26, 2023, the FDA issued a Warning Letter to Lone Star Botanicals, Inc.

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.

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.

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.

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.

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.

July 11, 2017

FDA Warns Dr. Carolyn Dean of Drug Claims Made for Magnesium, Calcium & Other Mineral Supplements

On June 27, 2017, the FDA issued a Warning Letter to Dr. Carolyn Dean of New Capstone, Inc.

February 13, 2018

American College of Sports Medicine Warns of Energy Drink Dangers

A new statement released by the American College of Sports Medicine (ACSM) highlights the dangers of energy drinks when consumed by children and adolescents, and calls for more studies on the safety and efficacy energy drinks.

April 29, 2014

Seller of B Vitamins, CoQ10, Amino Acids and Other Supplements Warned for Manufacturing Violations and Drug Claims

On April 1, 2014, the FDA issued a warning letter to Bio-Recovery, Inc.

March 11, 2017

Two Hospitalized After Drinking Herbal Tea With Aconite

On March 11, 2017 the San Francisco Department of Public Health announced that two people became ill and required intensive hospital care after consuming tea made from tea leaves purchased from Sun Wing Wo Trading Company in San Francisco.

March 11, 2024

Healthex Warned for Manufacturing Violations

On June 15, 2023, the FDA issued a Warning Letter to Healthex Distributors, Inc.

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.

February 07, 2012

Drug-Laced Supplements and Drink Mixes Recalled

According to the U.S. FDA, on February 3, 2012 Healthy People Co. announced a voluntary nationwide recall of several dietary supplements sold as capusules, drinks, and shake mixes. The supplements were found to contain drug substances and pose risks.

February 24, 2011

Recall of Counterfeit Extenze Tablets Containing Drugs

On February 23, 2011, the FDA announced that Biotab Nutraceuticals, Inc. was notified that two lots of counterfeit product purporting to be Extenze contain undeclared drug ingredients. Specifically, lot 0709241 contains tadalafil and sildenafil, and lot 0509075 contains tadalafil and sibutramine.

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 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:

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.

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.

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 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.

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.

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 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:

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

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.

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.

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:

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, ...

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: 

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:

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 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.

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.

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.

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.

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.

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 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.

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 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.

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.

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.

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.

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.

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.

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, ...

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.

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.

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.

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 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.

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 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.

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.

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.

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.

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.

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:

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.

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.

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.

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.

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 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

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

November 26, 2012

Court Injunction Halts Sale of Cholesterol, CoQ10, Progesterone, Prostate Supplements and More

On November 20, 2012, Pharmacist's Ultimate Health agreed to cease sales and distribution of its dietary supplements by entering into a Consent Decree of Permanent Injunction in the U.S. District Court of Minnesota.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

February 22, 2024

Pacific BioLogic Co. Warned by FDA for Manufacturing Violations

On December 21, 2023, the FDA issued a Warning Letter to Curtis Jacquot, dba Pacific BioLogic Co.

June 19, 2024

DBH Beverly Hills Sunscreen Falsely Promoted as Octinoxate Free, Says FDA

On June 12, 2024, the FDA issued a Warning Letter to Aqualex Co., Ltd.following inspection of the company’s website, manufacturing facility, and sunscreen products, which found its DBH Beverly Hills, EGF FGE DNA, UV Shield sunscreen to be misbranded.

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:

May 06, 2015

Joint Pain Supplements Found to Contain Diuretics, Antihistamines and Other Undeclared Drugs

On May 4, 2015, the FDA warned consumers not to buy or use the following supplements promoted for joint or back pain because they were found to contain undeclared drugs. Each was identified during an examination of international mail shipments.  

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.

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:

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:

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.

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.

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:

February 22, 2024

Herbalife Shake & Protein Drink Mix, Aloe, Linked With Case of Liver Injury

A 13-year-old boy in Texas developed liver failure and hepatitis-associated aplastic anemia after consuming two Herbalife products and an aloe vera beverage over a period of months, according to a report published on February 12, 2024 in the Journal of Pediatric Gastroenterology and ...

July 17, 2023

Seller of Ashwagandha, Lion’s Mane & Other Supplements Warned for Manufacturing Violations

On March 17, 2023, the FDA issued a warning letter to Brand Packaging Group, Inc. after FDA inspection of the company’s facility found products to be adulterated because they were prepared, packed, or held under conditions that do not meet Current Good Manufacturing Practices (CGMP).

July 19, 2023

FDA Warns Seller of Sleepy Time Products and Honey Herbal Syrups for Manufacturing Violations

On June 28, 2023, the FDA issued a warning letter to Eden’s Answers, Inc. after an inspection of the company’s facility found products to be adulterated because they were prepared, packed, or held under conditions that do not meet Current Good Manufacturing Practices (CGMP).

November 09, 2023

InnoMark Warned for Manufacturing & Misbranding Violations

On September 1, 2023, the FDA issued a Warning Letter to InnoMark, Inc.

July 25, 2024

West Coast Laboratories Warned for Manufacturing, Labeling Violations

On March 12, 2024, the FDA issued a Warning Letter to West Coast Laboratories, Inc.

September 24, 2024

Manufacturer of Mushroom Gummies Warned by FDA for Violations

On August 13, 2024, the FDA issued a Warning Letter to Restorative Botanicals, LLC, following an inspection of the company’s facility found the company’s products, including its My GUT Shrooms Gummies and My IMMUNE Shrooms Capsules, to be adulterated because they were prepared, ...

June 23, 2020

BioPure Healing Products Warned for Manufacturing Violations

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

March 31, 2020

Bulletproof Warned for Manufacturing Violations

On March 20, 2020, the FDA issued a warning letter to Bulletproof 360, Inc.

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.

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).

September 01, 2022

Elite One Source Nutritional Services Warned for Manufacturing, Labeling Violations

On August 5, 2022, the FDA issued a warning letter to dietary supplement manufacturer Nutritional Laboratories International, Inc. (DBA Elite One Source Nutritional Services, Inc.

March 23, 2023

FDA Warns Herbal Vitality for Promoting Supplements to Treat Cold & Flu, Kidney Stones & More

On March 7, 2023, the FDA issued a warning letter to Herbal Vitality, Inc.

January 26, 2023

FDA Warns Seller of Canary Seed Omega-3

On November 16, 2022, the FDA issued a warning letter to Evimeria El Aztecano, Inc. following review of the company’s Yerbas Finas Leche de Alpiste con Guanabana y Omega-3 product labeling, which found the product contained less magnesium and potassium than claimed on the label.

May 18, 2023

EarthLab, Inc. Warned for Promoting Green Tea, Curcumin, Elderberry & More to Treat Stroke, Cancer & Flu

On April 27, 2023, the FDA issued a warning letter to EarthLab, Inc., dba Wise Woman Herbals, following inspection of the company’s website which found statements about the company’s Green Tea Solid Extract, Curcuma Spp.

December 01, 2018

Seller of 5-HTP, Potassium & More Warned for Manufacturing Violations

On September 7, 2018, the FDA issued a warning letter to The Delano Company, Inc.

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:

April 27, 2023

Seller of Magtein, Veggie Caps, & More Warned for Drug Claims, Manufacturing Violations

On March 8, 2023, the FDA issued a warning letter to Spartan Enterprises Inc., dba Watershed Wellness Center, after a review of the company’s website found statements about its Dr. Bob’s Naturals Spirulina, Dr. Bob’s Naturals Magtein, Dr.

August 16, 2023

FDA Warns Sun Ten Laboratories for Manufacturing Violations, Drug Claims

On April 7, 2023, the FDA issued a warning letter to STPCA Inc. dba Sun Ten Laboratories because products were found to be adulterated because they were prepared, packed, or held under conditions that do not meet Current Good Manufacturing Practices (CGMP).

September 21, 2023

Moor Herbs, Inc Warned for Manufacturing Violations, Drug Claims

On August 1, 2023, the FDA issued a Warning Letter to Moor Herbs, Inc.

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.

July 26, 2023

Five Leaf Pet Botanicals Warned by FDA for Drug Claims

On June 22, 2023, the FDA issued a warning letter to Five Leaf Pet Botanicals, Inc.

November 18, 2024

Manufacturer of Grandma’s Herbs Kidney Warned by FDA

On October 20, 2023, the FDA issued a warning letter to Top Health Manufacturing, LLC, manufacturer of Grandma’s Herbs Kidney supplement, following an inspection of the company’s facility that found its products to be adulterated because they were, packed, labeled or held under ...

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.

April 17, 2024

FDA Warns Lipari Foods for Mislabeled Walnuts, Other Violations

On April 9, 2024, the FDA issued a Warning Letter to Lipari Foods Operating Company, LLC following multiple complaints and subsequent product recalls in August and September of 2023, which found the company did not follow the requirements of Current Good Manufacturing Practice (CGMP), Hazard ...

December 26, 2017

Seller of Fish Oil, Vitamin D, Whey Protein and More Warned for Manufacturing Violations

On December 19, 2017, the FDA issued a warning letter to Maine Natural Health, Inc.

July 07, 2020

Seller of Homeopathic Products Warned for Manufacturing Violations

On June 19, 2020, the FDA issued a warning letter to Washington Homeopathic Products, Inc.

November 24, 2021

FDA Warns Sanitizer Corporation For Manufacturing and Misbranding Violations

On September 24, 2021, the FDA issued a warning letter to Chameleon Beverage Co. Inc.

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.

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.

December 29, 2022

EarthLab, Inc. Warned for Promoting Curcumin, Elderberry to Treat Pain & Flu

On November 10, 2022, the FDA issued a warning letter to EarthLab, Inc., dba Wise Woman Herbals following inspection of the company’s website which found statements about the company’s products to be drug claims because they suggest the products can prevent or treat disease.

June 22, 2023

Nationwide Pharmaceutical’s Ferrous Sulfate Supplements Recalled

On June 22, 2023, the U.S.

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.

June 05, 2020

LifeHealth Science Warned for Manufacturing Violations

On May 15, 2020, the FDA issued a warning letter to LifeHealth Science, which found the company's ORËÁ product to be adulterated because it was prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.

September 01, 2020

Custom Nutraceuticals, LLC Warned for Manufacturing Violations

On August 6, 2020, the FDA issued a warning letter to Custom Nutraceuticals, LLC, following a facility inspection which found the company's products, including Thermal Revolution Black, Anabolic Blackout Raspberry Lemonade, Militia Re-COMP, and Rhino Rampage Wildberry to be ...

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.

August 25, 2022

Oregon’s Wild Harvest Warned by FDA for Manufacturing Violations

On July 8, 2022, the FDA issued a warning letter to Oregon’s Wild Harvest, Inc.

June 30, 2022

FDA Warns Seller of Vision and Allergy Supplements

On May 26, 2022, the FDA issued a warning letter to Golden Lab LLC following an inspection of the website, which found statements about the company’s DoctoRx’s Optimal Formula Ocular Pressure & Optic Nerve Support Formula Ocular Health Capsule, DoctoRx’s Optimal Formula ...

May 06, 2014

Seller of Flaxseed, Ginkgo and More Warned for Manufacturing Violations and Drug Claims

On April 18, 2014, the FDA issued a warning letter to Iowa Select Herbs, LLC, following a facility inspection which found the company's products, including Flax Seed, Holy Basil, Papaya Leaf Extract, and Ginkgo Leaf Extract products, to be adulterated because they were prepared, packed, or held ...

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 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 16, 2020

Seller of Silver, Arginine, and More Warned for Manufacturing Violations

On June 1, 2020, the FDA issued a warning letter to Morningstar Minerals LLC, which found the company's products, including Silver Boost, to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

September 08, 2020

FDA Warns Seller of Multivitamin for Manufacturing Violations

On August 14, 2020, the FDA issued a warning letter to Revival Products, Inc.

February 04, 2020

Seller of Digestion Supplements Warned for Manufacturing Violations

On January 10, 2020, the FDA issued a warning letter to Marco Pharma International LLC, which found the company's  Absinthium Herbal Liquid Extract 100 ml (Absinthium), promoted for "digestive support", and other products, including S21 Multi Somaplex 100 ml (Multi Somaplex), ...

February 18, 2020

Seller of CoQ10, Resveratrol and More Warned for Manufacturing Violations

On February 5, 2020, the FDA issued a warning letter to R-Garden LLC, which found the company's Vitamin O, Gamma-Zyme, L.

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.

December 17, 2020

FTC Crackdown on Six Deceptive CBD Products

On December 17, 2020, the FTC announced that it is taking action against six companies for selling CBD products with unsupported and deceptive health claims that they can treat a variety of conditions, including cancer, heart disease, hypertension, Alzheimer's disease, and others.

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 ...

March 31, 2005

FDA Warns Marketer of "Vitamin O" Product to Cease Unsubstantiated Claims

The U.S. Food and Drug Adminstration (FDA) has sent a Warning Letter (dated February 8, 2005) to Donald L. Smyth, President, R-Garden Inc., and Rose Creek Health Products, Inc. warning that its "Vitamin O" product was, among other things, being marketed with unsubstantiated health claims.

September 17, 2013

Seller of Omega-3 and Joint Supplements Warned for Manufacturing Violations and Drug Claims

On August 29, 2013, the FDA issued a warning letter to Y.S. Health Corp.

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.

May 10, 2013

Seller Of Sexual Enhancement and Hormonal Balance Supplements Warned For Manufacturing Violations

On April 26, 2013, the FDA issued a warning letter to Pristine Bay, L.L.C.

October 06, 2020

FDA Warns Seller of Red Yeast Rice, Vitamin D, Blood Pressure Supplements, and More

On August 28, 2020, the FDA issued a warning letter to Dr. Sam Robbins, Inc.

June 22, 2021

Living Free Vitamins, Joint, Nerve and Other Supplements Recalled

On June 21, 2021, Bea Lydecker's Naturals, Inc. issued a recall of six Living Free brand supplements because the labels do not declare soy lecithin.

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.

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 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.

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.

December 12, 2018

Seller of Protein Powder, Spirulina & Other Products Warned for Manufacturing Violations

On October 31, 2018, the FDA issued a warning letter to DynaPro International, Inc.

October 08, 2019

Seller of Tea, Colloidal Silver, Homeopathic Products Warned for Manufacturing Violations

On September 12, 2019, the FDA issued a warning letter to Herbal Healer Academy, Inc.

August 14, 2020

The Green Herb and New Genesis Health Warned for Manufacturing Violations

On July 31, 2019, the FDA issued a warning letter to Davis Ventures, Inc.

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.

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.

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 ...

June 07, 2017

FDA Warns Seller of Probiotic and Omega-3 Supplements for Manufacturing Violations

On May 22, 2017, the FDA issued a warning letter to BioTE Medical, LLC following a facility inspection which found its products, including BioTE DIM, BiotTE Probiotic, BioTE Iodine Plus, and BioTE Omega 3 to be adulterated because they were prepared, packed, or held under ...

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.

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.

August 20, 2019

Seller of Liposomal Curcumin, Vitamin C & Melatonin Warned for Manufacturing Violations

On August 6, 2019, the FDA issued a warning letter to Let's Talk Health, Inc.

October 15, 2020

FDA Warns Five Sellers of Dangerous Cesium Salt Supplements

On October 9, the FDA issued warning letters to five companies for selling products containing cesium chloride. The FDA has previously warned consumers not to use dietary supplements containing cesium chloride or any other cesium salt.

February 07, 2020

Cesium Salt Supplements Can Cause Heart Trouble, Death

On February 5, 2020, the FDA posted an alert warning consumers not to use dietary supplements containing cesium chloride or any other cesium salt.

June 09, 2020

Six More Multi-Level Marketing Companies Warned for Coronavirus and Deceptive Earnings Claims

On June 5, 2020, the FTC announced that it sent warning letters to six multi-level marketing companies for selling products such as immune system boosters and probiotics with unsupported claims that they can treat coronavirus (COVID-19) and/or for misrepresenting potential earnings people who have ...

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.

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 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, ...

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.

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 05, 2018

FDA Warns Seller of Colloidal Silver

On May 17, 2018, the FDA issued a warning letter to Silver Armor, Inc.

June 02, 2018

FDA Warns Seller of Cough Suppressant & Grape Seed Supplements

On March 29, 2018, the FDA issued a warning letter to Yoder's Good Health Products following a facility inspection which found a number of the company's products, including Respiratory & Cough Formula and Life Drops to be adulterated because they were prepared, packed, or ...

April 17, 2018

FDA Warns Seller of Echinacea, Iron, Aloe Supplements & More for Manufacturing Violations

On March 30, 2018, the FDA issued a warning letter to Ozark Country Herbs following a facility inspection which found a number of the company's products, including Echinacea-Goldenseal, Natural Iron, and Aloe-Vera Goldenseal Salve, to be adulterated because they were prepared, packed, or held under ...

April 17, 2018

Seller of Osha and Cayenne Supplements & More Warned for Manufacturing Violations

On March 21, 2018, the FDA issued a warning letter to Secret Garden of Health & Healing, LLC, following a facility inspection which found a number of the company's products, including Osha Root and Cayenne, to be adulterated because they were prepared, packed, or held under conditions that ...

September 25, 2018

Seller of B Vitamins, Multis, Glucosamine & More Warned for Manufacturing Violations

On August 31, 2018, the FDA issued a warning letter to Independent Nutrition Inc., following a facility inspection which the company's products, including  B-50 Complete, Multi-Vitamin & Mineral Complex (a.k.a.

October 24, 2012

Warning Issued to Memory Supplement Maker For Unapproved Drug Ingredient, Drug Claims and Unreported Adverse Events

On October 16, 2012, the FDA issued a letter to dietary supplement manufacturer Quincy Bioscience Manufacturing Inc.

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 ...

November 27, 2011

FDA Seeks Permanent Injunction Against Dietary Supplement Maker -- 400+ Products Affected

On November 23, 2011, the U.S. FDA took legal action against a dietary supplement maker and owner for substituting ingredients and products without noting the changes on the final product labels. The permanent injunction, filed on behalf of the FDA by the U.S.

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).

September 27, 2016

Seller of B Vitamins, Omega-3s and More Warned for Manufacturing Violations, Drug Claims

On September 15, 2016, the FDA issued a warning letter to Positive Power Nutrition, following a facility inspection which found the company's products, including High Energy C-Complex, Positive Vitality, Positive Performance, Positive CardioGuard, B-Complex 100, Positive Essentials, Positive ...

July 31, 2018

FDA Warns Seller of Joint Health and Cholesterol Supplements

On July 13, 2018, the FDA issued a warning letter to GC Natural, following a facility inspection which found a number of the company's products, including Red Pyrola Plus + Advanced Joint Formula Capsules, CSDP GOLD Capsules, Rejeune Optimal Kidney & Liver Support Extract balls, C.

July 18, 2018

Maker of Vitamin B12 and Multimineral Supplements Warned by FDA

On July 6, 2018, the FDA issued a warning letter to Aegle Nutrition, LLC, following a facility inspection which found some of the company's products, including Tropical Oasis Ionized Trace Minerals, Tropical Oasis Ultra Methyl B12, and Tropical Oasis Premium Vitamin B12 to be ...

July 03, 2018

FDA Warns Seller of Adulterated Chinese Herbal Supplements

On June 20, 2018, the FDA issued a warning letter to KPC Products, Inc.

March 31, 2018

Supplement Manufacturer Shut Down for Manufacturing Violations

On March 29, 2018, the FDA announced that U.S. District Court for the Eastern District of New York has entered a consent decree of permanent injunction with Riddhi USA, Inc. and Mohd M. Alam, president and owner of Riddhi USA, Inc., for selling adulterated and misbranded dietary supplements.

March 13, 2018

FDA Warns Seller of Milk Thistle, Chromium, Joint Supplements & More for Manufacturing Violations

On March 9, 2018, the FDA issued a warning letter to Carol Bond Health Foods following a facility inspection which found a number of the company's products, including Dolomite, Lipo Fat Fighter, ThistleX, Injuv, and Vinpocentine, to be ...

May 29, 2018

FDA Warns Seller of "Aromatase Inhibitor" Supplement

On May 18, 2018, the FDA issued a warning letter to Performance Nutrition Formulators LLC d.b.a. VMI Sports because its product Arimistane contains Androsta-3,5-Diene-7,17-Dione, an ingredient that the FDA considers to be a new drug and not a dietary supplement ingredient.

May 12, 2018

Seller of Astaxanthin, Cinnamon, Pine Bark and More Warned for Manufacturing Violations

On March 22, 2018, the FDA issued a warning letter to Get The Tea following a facility inspection which found the company's products, including Get the Tea Astaxanthin Max, Get the Tea Colostrum Complete, and Get the Tea Pine Bark Capsules, to be adulterated because they were ...

February 17, 2018

FDA Warns Seller Reishi Mushroom Supplements

On February 7, 2018, the FDA issued a warning letter to Reishi D. International, Inc., following a facility inspection which found the company's Reishi D.

January 13, 2018

Seller of Depression, Prostate Supplements & More Warned for Manufacturing Violations, Drug Claims

On August 21, 2017, the FDA issued a warning letter to Irmo-Vita, LLC, following a facility inspection which found that several of the company's products, including Hysta-Min, Man-Affirm, Phung-EX, and Bacto- EX to be adulterated because they were prepared, packed, or held ...

December 26, 2017

Seller of BrainAlert Warned for Manufacturing Violations, Drug Claims

On December 14, 2017, the FDA issued a warning letter to BrainAlert, LLC.

December 23, 2017

Seller of Meal Replacement, Protein Drinks, Cranberry and More Warned for Manufacturing Violations

On July 6, 2017, the FDA issued a warning letter to Professional Botanicals, Inc.

December 20, 2017

Seller of Supplements for Pain and Allergies Warned for Manufacturing Violations, Drug Claims

On December 13, 2017, the FDA issued a warning letter to GnuPharma Corporation, following a facility inspection which found a number of the company's products, including Relief capsules, Foundation capsules, Aller-geez capsules, Fit capsules, Aller-Geez Tea, Foundation herbal tea and ...

August 12, 2019

Miracle Mineral Solution Is Dangerous, Warns FDA

On August 12, 2019, the FDA warned consumers not to buy or use Miracle Mineral Solution or other "Miracle" or "Master" solution products containing sodium chlorite because they can dangerous and even life-threatening reactions.

July 16, 2019

FDA Warns Seller of Magnesium and CBD

On July 9, 2019, the FDA issued a warning letter to Ceba-Tek, Inc.

December 27, 2012

Two Supplement Companies Warned For Manufacturing Violations

Sterling USA Neutraceutical Lab, LLC -- On November 16, 2012, the FDA issued a warning letter to Sterling USA Neutraceutical Lab, LLC following a facility inspection which found the company’s dietary supplements to be adulterated because they were have been prepared, packed, or held under ...

April 11, 2008

Twelve Dietary Herbal Supplements Recalled -- Possible Health Risk Associated with Ephedra, Aristolochic Acid and Human Placenta

On April 10, 2008, the FDA posted a recall notice issued the same day from Herbal Science International, Inc. (AKA Jen-On Herbal Science International, Inc.).

February 20, 2013

Cold, Flu and Stress Supplement Company Warned For Adulteration, Drug Claims And More

On October 5, 2012, the FDA issued a warning letter to dietary supplement manufacturer Wholistic Herbs, Inc. following a facility inspection which found the company's products, including At-Ease, Morning Calm, Aller-Ban, Stomach Flu, Kold & Koff, Kold Sore, and L.

July 28, 2008

Seizure of Xiadafil VIP Tablets After Company Refuses Recall

On July 24, 2008, the FDA announced that U.S. Marshals seized nearly $74,000 worth of Xiadafil VIP tablets, Lots 6K029 and 6K209-SEI, distributed by SEI Pharmaceuticals, Inc. of Miami, Fla.

February 13, 2013

Herbal Supplement Maker Warned For Manufacturing Violations, Misbranding

On February 6, 2013, the FDA issued a warning letter to Genesis Herb Company LLC, following a facility inspection which found the company's Seizure, Relax, Formula ARTH, Disintegrate, Gout, Plantain, and Colloidal Silver dietary supplements to be adulterated because they were prepared, packed, or ...

August 28, 2013

Maker of Sexual Enhancement Supplement Warned for Manufacturing Violations

On July 11, 2013, the FDA issued a warning letter to Precise Nutrition International Inc.

March 14, 2012

Manufacturing Violations by Maker of Lecithin, Soy Supplements

The FDA issued a Warning Letter (dated March 7, 2012) to Modern Products, Inc. regarding manufacturing violations in the production of the supplements Fearn Lecithin Granules, Fearn Liquid Lecithin, Fearn 100% Soy Protein Isolate, and Gayelord Hauser Brewers Yeast.

April 07, 2011

FDA Warns Manufacturer of Soy Products of Violations

The U.S. FDA published a Warning Letter on dated March 25, 2011 to Soluble Products Co., LP, regarding serious violations of Current Good Manufacturing Practices (cGMPs) in its production of Revival brand products.

July 01, 2014

Maker of Elderberry Concentrate Warned for Manufacturing Violations

On June 23, 2014, the FDA issued a warning letter to Wyldewood Cellars Inc.

August 26, 2014

Supplement Maker Warned for Manufacturing Violations

On August 14, 2014, the FDA issued a warning letter to dietary supplement manufacturer Big Easy Confections following a facility inspection which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing ...

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.

September 10, 2013

CoQ10 and Carnitine Supplement Company Warned For Manufacturing Violations

On April 15, 2013, the FDA issued a warning letter to Irenda Corporation, following a facility inspection which found the company's products, including L-Carnitine, Acetyl L-Carnitine, and Co-Q 10 with L-Carnitine, to be adulterated because they were packed, or held under conditions that violate ...

March 13, 2013

Liquid Supplements Not Properly Manufactured Despite Certification

On February 22, 2013, the FDA issued a warning letter to Organics Corporation of America, dba Ambix Laboratories, following a facility inspection which found the company's dietary supplements Baby Plex Vitamin Drops, Carnitine Liquid, and Optimal Nutritional Liquid to be adulterated because they ...

September 25, 2018

FDA Warns Seller of Digestive Enzyme Supplements

On March 6, 2018, the FDA issued a warning letter to Uckele Health & Nutrition, Inc.

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.

July 23, 2016

Maker of "Super Food" Warned for Manufacturing Violations

On July 12, 2016, the FDA issued a warning letter to TerraVare, Inc.

June 06, 2017

Seller of Herbal Supplements Warned for Manufacturing Violations, Drug Claims

On May 25, 2017 the FDA issued a warning letter to Life Rising Corporation, following a facility inspection which found the company's products, including Stomach Regulator, Fang Feng Formula, Skin Regulator, Regulate Liver, Circulation Regulator, Pancreas Support, Lung Regulator, Pure Tea, ...

July 18, 2017

FDA Warns Seller of "Quick Slim with pure Hoodia Gardonii" and "Diabalance Herbal Blood Sugar Balance"

On July 11, 2017, the FDA issued a warning letter to Black Seed Herb, Inc.

March 02, 2013

FDA Finds Manufacturing Violations At NSF-Certified Supplement Facility

The FDA recently warned dietary supplement manufacturer Beehive Botanicals, Inc.

March 22, 2013

Maker of Nutrition Shakes Warned For Manufacturing Violations

On February 28, 2013, the FDA issued a warning letter to Healthwest Minerals, Inc., dba Mt. Capra Products, Mt. Capra Whole Foods, and Mt.

April 11, 2013

Glutathione Supplement Maker Warned For Manufacturing Violations and Drug Claims

On April 5, 2013, the FDA issued a warning letter to The Glutathione Corporation following a facility inspection which found the company's supplements, including Ultrathione 500 Glutathione, Ultrathione 1000 Sports Pack, Ultrathione Performance, Ultrathione Extreme Performance, Ultrathione Health ...

April 11, 2013

Chinese Herbal Manufacturer Warned For CGMP Violations

On March 20, 2013, the FDA issued a warning letter to Finemost Corporation, dba Qualiherb, following a facility inspection which found the company's supplements, including Yi Zhi Tang and C.

February 14, 2013

Maker of Antioxidant and Anti-Aging Supplements Warned For Manufacturing Violations

On January 10, 2013, the FDA issued a warning letter to dietary supplement manufacturer Consolidated Marketing Unlimited, Inc.

April 18, 2013

Cardio, Energy and Sexual Enhancement Supplement Distributor Warned For Manufacturing Violations and Drug Claims

On December 21, 2012, the FDA issued a warning letter to ForMor Inc, dba ForMor International, following a facility inspection which found the company's Cardio Cocktail and Argenix dietary supplements to be adulterated because because they were prepared, packed, or held under conditions that do ...

May 23, 2013

Maker of Liver Detox and Insulin Supplements Warned For Drug Claims

On April 24, 2013, the FDA issued a warning letter to Glucorell, Inc.

May 17, 2013

Maker of Cardio, Arthritis, Cleanse Supplements and More Warned For Manufacturing Violations and Drug Claims

On May 8, 2013, the FDA issued a warning letter to Entrenet Nutritionals, Inc.

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.

October 05, 2011

FDA Warns Herbal Nitro of Manufacturing Violations

The FDA has published a Warning Letter dated September 22, 2011 to Herbal Nitro Inc. regarding manufacturing violations at its facility in Yucaipa, CA.

July 12, 2013

Herbal Supplement Company Warned For Drug Claims, Manufacturing Violations

On June 18, 2013, the FDA issued a warning letter to Herbs of Light, Inc.

August 21, 2014

Seller of Joint Supplement Warned for Manufacturing Violations and Drug Claims

On July 17, 2014, the FDA issued a warning letter to Klein Laboratories, Inc.

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.

January 21, 2015

Supplement Maker Ordered to Stop Selling Products

On January 15, 2015, a federal judge ordered a permanent injunction against dietary supplement manufacturer Health One Pharmaceuticals, Inc. which requires the company to stop manufacturing and selling dietary supplements.

December 05, 2014

Maker of Immune Supplement Warned for Manufacturing Violations

On November 20, 2014, the FDA issued a warning letter to Urban Moonshine, Inc.

July 15, 2014

Pinnacle Labs International Warned for Manufacturing Violations

On June 24, 2014, the FDA issued a warning letter to Pinnacle Labs International, Inc.

July 15, 2014

Vita Springs Health Warned for Manufacturing Violations and Drug Claims

On June 24, 2014, the FDA issued a warning letter to Albert Max Inc.

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.

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.

August 01, 2013

Maker of Algae Products Warned For Drug Claims, Manufacturing Violations

On March 8, 2013, the FDA issued a warning letter to Algaen Corporation following a facility inspection and website review which found statements made about the company's AlgaBerry products to be drug claims. 

August 06, 2013

Maker of Greens and Whole Foods Supplements Warned For Drug Claims, Manufacturing Violations

On July 19, 2013, the FDA issued a warning to ProNatural Nutrition, LLC, following a facility inspection which found that statements made on product labels, including "Healing to cells and tissues," and "Non-toxic antibiotic" to be drug claims.

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 05, 2014

Seller of Aloe and Vitamin C Supplements Warned for Manufacturing Violations

On December 12, 2013, the FDA issued a warning letter to Health Breakthroughs International, following a facility inspection which found the company's products, MPS Gold 100, MPS Gold 3X and Amazing C, to be adulterated because they were prepared, packed, or held under conditions that violate ...

May 03, 2013

Maker of Probiotic, Iron and Folic Acid Supplements Warned For Manufacturing Violations

On April 17, 2013, the FDA issued a warning letter to Hillestad Pharmaceuticals USA, Inc.

May 24, 2013

Brewable Tea and Tea Supplement Company Warned For Manufacturing Violations and Drug Claims

On April 2, 2013, the FDA issued a warning letter to Natures Health Options, LLC, following an investigation which found the company's Charantea Bitter Melon Ampalaya, which is distributed as a dietary supplement in capsule form, and as a tea, to be adulterated because it was prepared, packed, or ...

February 28, 2013

Maker of Liquid Omega-3 Supplements Warned For Manufacturing Violations

On February 20, 2013, the FDA issued a warning letter to Capco Custom Packaging Inc.

November 22, 2017

FDA Warns Distributor of "Testosterone Wellness for Men"

On November 8, 2017, the FDA sent a warning letter to Vita-Pure, Inc.

March 08, 2016

Maker of Calcium and Vitamin C Supplements Warned for Manufacturing Violations

On September 17, 2015, the FDA issued a warning letter to Raphah, Inc.

June 07, 2013

Seller of Red Rice Yeast With CoQ10, Respiratory Supplement And More Warned For Manufacturing Violations and Drug Claims

On February 25, 2013, the FDA issued a warning letter to Altasource, LLC, dba Meta Labs LLC, following a facility inspection which found the company's dietary supplements, including Respiratory Response, African Mango, Coffee Black Salve, Meta-Cell, Conjugated Linoleic Acid and Red Yeast Rice with ...

August 16, 2013

Ginkgo, Milk Thistle, Cleanse and Nopal Supplement Maker Warned For Manufacturing Violations, Drug Claims

On July 23, 2013, the FDA issued a warning letter to Natural Products Services, Inc.

November 06, 2014

Seller of Prostate, Heart Supplements and More Warned for Drug Claims

On October 9, 2014, the FDA issued a warning letter to Health Research Laboratories, LLC/New World Health, following a review of the company's websites, which found statements made about AtheChel Advanced, Betarol, BioTherapex, Omega-3 Cardio Plus, RejuvaLifeRx, and Ultimate Health Formula to be ...

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.

January 07, 2002

Liver Toxicity with Kava

As announced in a December 19, 2001 letter to healthcare professionals, The Food and Drug Administration (FDA) is investigating whether the use of dietary supplements containing kava (also known as kava kava or Piper methysticum) is associated with liver toxicity.

May 25, 2013

70% of Dietary Supplement Company FDA Inspections Find Potential Manufacturing Violations

Seventy percent of dietary supplement facilities inspected by the FDA over a 3 year period (444 facilities out of 626) were cited for violating federal regulations, known as dietary supplement Current Good Manufacturing Practices (cGMPs), according to information received by Natural Products ...

May 24, 2013

Seller of Liquid Minerals, Joint Care and Herbal Supplements Warned For Manufacturing Violations, Drug Claims

On April 8, 2013, the FDA issued a warning letter to Body Systems, Inc.

June 07, 2013

Maker of Colloidal Silver and Mushroom Extract Supplements Warned For Manufacturing Violations and Drug Claims

On May 2, 2013, the FDA issued a warning letter to Earthborn Products, Inc.

February 28, 2013

Maker of Joint, Mood and B Vitamin Supplements Warned For Manufacturing Violations, Misbranding and Drug Claims

On February 11, 2013, the FDA issued a warning letter to Kreativ Health, Inc.

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 ...

April 11, 2013

Maker of Workout Booster Warned For Manufacturing Violations

On March 5, 2013, the FDA issued a warning letter to Primarch Manufacturing, Inc.

May 18, 2012

Caution with Butterbur Indicated by UK Warning

England's Medicines and Healthcare Products Regulatory Agency (MHRA) advised consumers in early 2012 not to take unlicensed butterbur (Petasites hybridus) herbal products due to potential health risks.

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.

October 31, 2014

Seller of "Cleanse," Allergy Supplements and More Warned for Manufacturing Violations, Drug Claims

On October 15, 2014, the FDA issued a warning letter to Evangelical Christian Ministries, dba Health & Herbs, following a facility inspection which found the company's products, CORYDALIS and CVF BGONE to be adulterated because they were prepared, packed, or held under conditions that violate ...

October 30, 2014

Supplement Maker Warned for Manufacturing Violations

On October 21, 2014, the FDA issued a warning letter to DNG Trading & Milling, LLC, following a facility inspection 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 ...

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.

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, ...

January 17, 2015

Supplement Maker Warned for Manufacturing Violations

On August 5, 2014, the FDA issued a warning letter to Engineering Nutrition, following a facility inspection which found the company's products, which were not named, to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for ...

January 17, 2015

Maker of Magnesium and Potassium Supplements Warned for Manufacturing Violations

On December 23, 2014, the FDA issued a warning letter to Nutri Spec, Inc.

December 30, 2014

Maker of Probiotic Supplement Warned for Manufacturing Violations

On December 18, 2014, the FDA issued a warning letter to Wellmill LLC, dba Vitamix, following a facility inspection which found the company's products, including Butcher's Broom powder and Lactobacillus acidophilus powder (used as ingredients in a finished product which was not named) to be ...

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 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 ...

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.

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 23, 2015

Maker of Vitamin Drinks Warned for Manufacturing Violations

On January 7, 2015, the FDA issued a warning letter to NYSW Beverage Brands, Inc.

December 05, 2014

Maker of Ginseng, Zinc, Calcium and More Warned for Manufacturing Violations

On November 20, 2014, the FDA issued a warning letter to Long Island Pharmaceuticals, LLC, following a facility inspection 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 ...

December 12, 2014

Seller of Omega-3 "Syrup" Warned for Manufacturing Violations and Drug Claims

On October 16, 2014, the FDA issued a warning letter to Mr.

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.

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.

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 ...

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 ...

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.

August 11, 2015

Company Ordered to Stop Making and Selling Supplements

On August 4, 2015, a federal court ordered a permanent injunction against dietary supplement company Atrium Inc., and two companies under the same ownerhship, Aspen Group Inc., Nutri-Pak of Wisconsin 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 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 19, 2014

Seller of Sexual Enhancement Supplements Warned For Manufacturing Violations

On February 11, 2014, the FDA issued a warning letter to Maximus Niterider International Group, 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.

February 13, 2014

Seller of Iron, Prostate, Valerian and Other Supplements Warned For Multiple Violations and Drug Claims

On January 31, 2014, the FDA issued a warning letter to NatureAll-STF Holding, LLC, following a facility inspection which found the company's products, including Colostrum, Valerian-Plus, Wormwood, Black Walnut-Plus, Lung-Plus, Yucca-Plus (Arthro Plus), Iron Plus, MSM Plus, White Willow Plus, ...

February 05, 2014

Maker of Digestive Health Supplement Warned For Manufacturing Violations, Drug Claims

On January 22, 2014, the FDA issued a warning letter to Intensive Nutrition Incorporated, following a facility inspection which found the company's digestive support supplement, Tanalbit, to be adulterated because it was prepared, packed, or held under conditions that violate Current Good ...

January 16, 2014

Seller of Tea Supplements and Drinks Warned For Manufacturing Violations and Drug Claims

On December 31, 2013, the FDA issued a warning to Prestige Chinese Teas Company, Inc.

August 26, 2014

Maker of Herbal Supplements Warned for Manufacturing Violations and Drug Claims

On August 8, 2014, the FDA issued a warning letter to EnerHealth Botanicals, LLC following a facility inspection which found the company's products, including Parasite Purge Herbal Remedy, Black Walnut Extract, Bladder Cleanse Herbal Extract, Lung Renewal Herbal Remedy, EchinOsha and Daily Immune ...

May 21, 2014

Seller of Gingko and Milk Thistle Warned for Manufacturing Violations and Drug Claims

On April 4, 2014, the FDA issued a warning letter to Xtra Life Natural Systems, Inc.

August 06, 2014

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

On July 25, 2014, the FDA issued a warning letter to Mezotrace Corporation following a facility inspection which found the company's products, including Calcium/Magnesium Natural Minerals & Trace Elements, Calcium/Magnesium Natural Minerals & Trace Elements with Vitamin D, and Calcium/Magnesium ...

July 24, 2014

Seller of Noni Juice Products Warned for Manufacturing Violations, Drug Claims

On July 14, 2014, the FDA issued a warning to Noni Connection dba Puna Noni, following a facility inspection which found the company's Puna Noni 100% Pure Hawaiian Noni Fruit Capsules to be adulterated because they were prepared, packed, or held under conditions that violate Current Good ...

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 ...

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.

March 08, 2016

Seller of Echinacea Warned Manufacturing Violations, Drug Claims

On February 25, 2016, the FDA issued a warning letter to Herbal Energetics/ In Joy Organics, following a facility inspection which found the company's product, X Out-Rays to be adulterated because it was prepared, packed, or held under conditions that violate Current Good ...

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.

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.

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.

October 08, 2016

Seller of Cell Power and Super Silica Warned for Manufacturing Violations, Misbranding

On September 23, 2016, the FDA issued a warning letter to SSO, Inc.

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 ...

November 25, 2017

Seller of "BounceBack" Joint Supplement and Others Products Warned for Drug Claims

On November 14, 2017, the FDA sent a warning letter to Mannatech Incorporated following a facility inspection that found the products BounceBack, MannaBears, ImmunoSTART, TruSHAPE, and Catalyst to be in violation of the Current Good Manufacturing ...

May 30, 2017

Maker of Collagen Supplement Warned for Manufacturing Violations

On July 17, 2014, the FDA issued a warning letter to Morhaim Pharmalab, Inc.

April 04, 2017

Seller of B Vitamins, Vitamin C, Potassium & More Warned for Manufacturing Violations

On March 24, 2017 the FDA issued a warning letter to The Sanapac Company, Inc.

April 01, 2017

Maker of Prelief, Urinozinc Prostate Health Formula Warned for Manufacturing Violations

On March 16, 2017 the FDA issued a warning letter to DSE Healthcare Solutions, LLC, following a facility inspection which found the company's products, including Prelief and Urinozinc Prostate Health Formula to be adulterated because they were prepared, packed, or held under ...

January 07, 2017

Seller of Protein and Workout Supplements Warned for Manufacturing Violations, Label Errors

On December 22, 2016, the FDA issued a warning letter to Rock Solid Nutrition, LLC, following a facility inspection which found the company's products, including  Whey Isolate (Cinnabun flavor), Pre-Pump (Massive Mango flavor)  and Strength Test to be adulterated because ...

February 16, 2017

U.S. Department of Justice Files Permanent Injunction Against Supplement Manufacturer

On February 16, 2017, the United States Department of Justice filed a complaint against Pick and Pay, Inc.

February 07, 2017

Seller of Chinese Herbal Products for Prostate, Menopause and More Warned for Manufacturing Violations

On January 23, 2017, the FDA issued a warning letter to Herbal Sciences International, Inc.

March 14, 2017

Court Shuts Down Supplement Manufacturer

On March 13, 2017, the U.S. District Court for Colorado ordered dietary supplement manufacturers and distributors  EonNutra LLC, CDSM LLC and HABW LLC, and their owner, Michael Floren, to stop all operations until they come into compliance with federal regulations. 

June 26, 2006

FDA Warns Candy Maker Making Heart Health Claims

On May 31, 2006, the U.S.

November 28, 2014

Seller of Herbal Extracts Warned for Manufacturing Violations, Drug Claims

On November 3, 2014, the FDA issued a warning letter to Avena Botanicals, Inc.

November 21, 2014

Seller of Diabetes, Prostate Supplements and More Warned for Manufacturing Violations, Drug Claims

On October 7, 2014, the FDA issued a warning letter to dietary supplement distributor Windmill Health Products, LLC, following a facility inspection which found the company's products, including Nutri-Betic caplets, Vita-betic caplets, ProstrinRx tablets, Polyflavanol capsules, and Glucoflex Joint ...

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.

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.

June 23, 2017

FDA Warns Seller of Menopause, Sexual Enhancement, Prostate Supplements and More For Manufacturing Violations

On May 26, 2017 the FDA issued a warning letter to Star Health & Beauty LLC, following a facility inspection which found the company's products, including Nu Essentials Royal Jelly Capsules, NuMan Male Enhancement Capsules, Star's Male Potency Tonic, NuGen HP, She Max HP, and V Max ...

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, ...

July 29, 2009

FDA Warns Against Body Building Supplements with Steroid-like Compounds

On July 28, 2009, the U.S. FDA notified the public about new safety information concerning products marketed for body building and increasing muscle mass.

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.

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.

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.

May 03, 2013

Maker of Omega-3, Saw Palmetto, St. John’s Wort Supplements And More Warned For Manufacturing Violations and Drug Claims

On March 19, 2013, the FDA issued a warning letter to Sunset Natural Products Inc.

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.

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 ...

October 30, 2014

Seller of Vitamin C, Iron and Detox Supplements Warned for Violations, Drug Claims

On October 16, 2014, the FDA issued a warning letter to Vitalab Co., Inc. (which manufactures and labels supplements for three distributors: V.E. Irons, Inc., Springreen Products, Inc., and Sonne's Organic Foods, Inc.

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.

October 03, 2014

Seller of Green Tea, Prostate, Pain Supplements and More Warned for Manufacturing Violations and Drug Claims

On July 25, 2014, the FDA issued a warning letter to AMS Health Sciences, LLC following a facility inspection which found the company's products, including saba ACE, UROPOWER, UROSure, Digest-Eze, Shark Cartilage, Colloidal Silver, and Mobilite to be adulterated because they were prepared, packed, ...

April 16, 2014

Seller of Aloe, Thyroid and Other Supplements Warned for Manufacturing Violations and Drug Claims

On March 21, 2014, the FDA issued a warning letter to Aloe Man International Corp.

October 24, 2012

Manufacturer of Green Tea, Vitamin E, Omega-3 and Cranberry Supplements Warned For Manufacturing Violations, Misbranding and Drug Claims

On October 16, 2012, the FDA issued a warning letter to dietary supplement manufacturer Advanced Nutritional Technology Inc.

October 25, 2016

Seller of Liquid Aloe & Mineral Supplement Warned for Manufacturing Violations

On August 10, 2016, the FDA issued a warning letter to Perfect Source Natural Products Inc.

February 28, 2017

Seller of Tea Supplements Warned for Manufacturing Violations

On February 3, 2017, the FDA issued a warning letter to Kumato Labs, following a facility inspection which found the company's products, including CHO WA Tea, COMOXIN IBS Formula and NEMURI Sleep Formula to be adulterated because they were prepared, packed, or held under ...

April 04, 2012

Maker of Protein Drinks and Supplements Warned of Manufacturing Violations

The FDA published a Warning Letter to Protica, Inc., a maker of protein drinks and supplements, regarding violations of manufacturing regulations discovered during inspection of its facility in Whitehall, PA. Affected products include the foods Amped Up-2oz, Fireball-2oz, Healthy Shot-2.

August 09, 2012

FDA Warns Sports Nutrition Manufacturer of GMP Violations

On June 26, 2012, the FDA issued a warning letter to Parrillo Performance subsequent to a manufacturing and packing facility inspection which found Parrillo products to be adulterated due to current Good Manufacturing Practices (cGMP) violations.

November 30, 2011

Maker of Acai Product Warned by FDA of Manufacturing Violations

The U.S. FDA recently published a Warning Letter to Precision Formulations, LP (Coppell, Texas) dated 10/24/11, indicating that a recent inspection of its facility found violations of the Current Good Manufacturing Practice reguations for dietary supplements.

March 03, 2012

FDA Warns Vitaganic of Manufacturing Violations

On February 8, 2012, the U.S. FDA sent a Warning Letter to Vitaganic, Inc. regarding violations of Current Good Manufacturing Practic (CGMP) regulations for dietary supplements found during an inspection of it manufacturing facility in Sunnyvale, California in October 2011.

October 08, 2010

FDA Warns of Stimulant in Slimming Capsules

On October 8, 2010, the U.S. FDA advised consumers who have Slimming Beauty Bitter Orange Slimming Capsules not to use the product. FDA warns that Slimming Beauty Bitter Orange Slimming Capsules contain the active pharmaceutical ingredient sibutramine, a prescription-only drug which is a stimulant.

February 06, 2013

Vitamin and Supplement Maker Warned For Labeling Errors, Manufacturing Violations

On January 25, 2013, the FDA issued a warning letter to NX Generation Ltd.

September 13, 2010

ExtenZe Enhancement Supplements Seized in Canada

On August 19, 2010, Health Canada (Canada's health ministry) seized the sexual enhancement supplements "Male Enhancement ExtenZe" and "Women ExtenZe" which were imported from the U.S. Although legal and widely sold in the U.S.

April 07, 2010

Nationwide Recall of Masxtreme Capsules Containing Drugs with Cardiovascular Side Effects

On March 30, 2010, the U.S. Food and Drug Administration (FDA) posted a notice from Natural Wellness warning consumers not to purchase or consume the product known as MasXtreme, Lot# 911035.

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.

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.

October 09, 2013

Use of Chinese Supplement Linked to Rare But Serious Condition

On October 9, 2013, Health Canada warned consumers that Compound Danshen Dripping Pills, manufactured by Tianjin Tasly Pharmaceutical Co., have been associated with a case of methemoglobinemia, a rare but serious condition which may result in coma or death.

July 05, 2012

FDA Warns Good Herbs Inc. of Manufacturing Violations and Drug Claims

The FDA issued a warning letter to Good Herbs Inc. on May 24, 2012, after a facility inspection found the company to be in violation of current manufacturing regulations, including lack of documentation and written procedures.

May 07, 2012

FDA Warns Doctor Promoting Own Supplements Online as Treatments

On April 18, 2012 the U.S. Food and Drug Administration (FDA) sent a Warning Letter to Jacob Teitelbaum, M.D. of Fatigued to Fantastic, LLC regarding the promotion that company's products on its website www.endfatigue.com.

September 27, 2010

FTC Charges Deceptive Advertising by POM Wonderful

On September 27, 2010, the U.S.

June 15, 2003

FTC Alleges "Heartbar" Made Deceptive Claims About Effectiveness

On June 12, 2003, the Federal Trade Commission (FTC) announced that Unither Pharma, Inc. and United Therapeutics Corporation have agreed to settle FTC charges that they made deceptive claims in advertising for their HeartBar product.

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 ...

September 26, 2014

Sellers of Essential Oils Warned for Claiming to Treat Ebola, Other Diseases

On September 22, 2014, the FDA issued a warning to Young Living following a review of websites, Pinterest, Facebook and Twitter accounts owned by Young Living distributors, which found statements made about the company's essential oils, including Thieves, Cinnamon Bark, Oregano, ImmuPower, ...

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.

March 15, 2013

Maker of Liquid Supplements Warned For Manufacturing Violations and Drug Claims

On January 31, 2013, the FDA issued a warning letter to Liquid Health, Inc.

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).

March 28, 2011

Dangerously High Levels of Vitamins A and D in Product Prompt FDA Warning

On March 28, the U.S. FDA warned consumers to stop using Soladek, a vitamin-solution product marketed by Indo Pharma, S.A., of the Dominican Republic, because the product may contain dangerously high levels of vitamins A and D.

July 06, 2012

Centrum Multivitamins: Breast and Colon Health Claims Pulled

On July 5, 2012, Pfizer Consumer Healthcare announced it will withdraw breast and colon health claims from its Centrum multivitamin advertising and labels, and will revise health and energy claims made on other Centrum products.

January 18, 2013

FTC Upholds Ruling, POM Wonderful Health Claims Were Deceptive

On January 16, 2013, the Federal Trade Commission (FTC) announced it will uphold a judge’s ruling that makers of POM Wonderful 100% Pomegranate Juice and POMx supplements made deceptive and unsubstantiated claims that the products could treat, prevent, or reduce the risk of heart disease, prostate ...

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.

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.

July 28, 2015

Abnormal Heart Rhythms Linked with Unauthorized Natural Product, Health Canada Warns

On July 27, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced that it has received a serious adverse reaction report of abnormal heart rhythms associated with the use of an unauthorized natural product in Canada called Remogen, which contains the drug ibogaine.

May 30, 2017

Seller of Vitamin C, Calcium, Mushroom Supplements and More Warned for Manufacturing Violations

On May 12, 2017 the FDA issued a warning letter to VitaPurity Corporatio.

July 18, 2017

Seller of "Super Strength Prostate Formula," Acai Berry Supplements & More Warned for Drug Claims

On June 30, 2017, the FDA issued a warning letter to Nature's Health Company, LLC, following a facility inspection and review of the company's website, www.natureshealthcompany.

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.

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.

May 23, 2013

Seller of Sexual Enhancement, Cholesterol, Resveratrol Supplements and More Warned For Drug Claims

On May 2, 2013, the FDA issued a warning letter to Alternative Health Supplements, following a review of the company's website, which found statements made about several dietary supplements, including Regenerect, Alligin, Astaxanthin Advantage, HDL Cholesterol Management, Resveratrol, Coral Calcium ...

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 ...

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.

March 30, 2016

Toxins in Chocolate

On March 23, 2016, As You Sow, a consumer health watchdog group based in California, released results showing that 35 of 50 chocolate products it tested, including chocolate bunnies and eggs, expose consumers to lead and cadmium above levels set by California's Safe Drinking Water and Toxic ...

September 28, 2017

Seller of Prostate, Reishi Supplements Warned for Manufacturing Violations

On September 11, 2017, the FDA issued a warning letter to Vicare International (USA), Inc.

August 29, 2017

FDA Warns Seller of Supplements for Allergies, Joint Pain, Bone Health, and More

On August 16, 2017, the FDA issued a warning letter to Total Nutrition, Inc.

June 27, 2017

Seller of Alpha Lipoic Acid, Cinnamon Supplements and More Warned For Manufacturing Violations

On May 1, 2017 the FDA issued a warning letter to Nature's Vision, Inc.

May 02, 2017

Seller of Amino Acid Supplements & More Warned for Manufacturing Violations

On April 20, 2017 the FDA issued a warning letter to Naturecom Inc.

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.

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 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.

March 28, 2011

FDA Cracks Down on Violators of Supplement Manufacturing Rules

In February and March 2011, the U.S. FDA posted Warning Letters sent, respectively, to a distributor of dietary supplements and a supplement manufacturer for violations of current Good Manufacturing (GMP) rules.

September 20, 2010

Many Supplements Recalled for Hormone-Affecting Compounds

On September 20, 2010, the U.S. FDA posted a Safety Notice regarding the recalls of several products marketed as dietary supplements that contain aromatase inhibitors, commonly known as "ATD.

September 15, 2010

Recall of Testosterone-Boosting Supplement

On September 14, 2010, the FDA posted a notice that KiloSports is recalling Clomed (60 count bottles), a supplement with claims to "release gonadatropin," "elevate testosterone" and "promote spermatogenesis."

July 15, 2011

FDA Inspection Finds Manufacturing Problems with Several Supplements Including Women's Multivitamin

The U.S. FDA recently posted a Warning Letter sent to BioSan Laboratories of Derry, New Hampshire on June 17, 2011 concerning multiple violations of Good Manufacturing Practice regulations and labeling rules.

April 30, 2003

Massive Recall by Australian Supplement Maker

On April 28, 2003, Australia's Therapeutic Goods Administration (TGA) suspended the licence held by Pan Pharmaceuticals Limited of Sydney to manufacture medicines, for a period of six months with effect 28 April 2003, because of serious concerns about the quality and safety of products manufactured ...

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.

August 19, 2015

Soylent Meal Replacement Powder Reported to Contain Lead and Cadmium

On August 13, 2015, an environmental-health watchdog group, As You Sow, filed a notice of intent to bring legal action against Soylent, a "meal replacement" powder, alleging violation of California's "Prop 65" Safe Drinking Water and Toxic Enforcement Act ...

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.

October 16, 2014

Seller of Black Cohosh, Ginkgo and More Warned For Manufacturing Violations and Drug Claims

On April 2, 2014, the FDA issued a warning letter to Pure Herbs, Ltd.

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 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.