Product Reviews and Information for High Blood Pressure

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.

May 24, 2023

Seller of Echinacea, High Blood Pressure Products & More Warned for Drug Claims

On May 12, 2023, the FDA issued a warning letter to H.E.A.L.

August 16, 2023

FDA Warns Hekma Center, LLC for Promoting Products to Treat Anemia, Diabetes, Depression, & More

On June 2, 2023, the FDA issued a warning letter to Hekma Center, LLC following review of the company’s website and social media, which found statements about the company’s Natural Supplements for Anemia, Lymf (Galium aparine), Natural Supplements for Cardiomyopathy, Magic1 (Moringa ...

July 15, 2024

Hard Steel Supplements for Men Recalled

On July 12, 2024, Supercore Products Group issued a recall of Hard Steel Capsules and Gold Hard Steel Liquid which are used for male erectile dysfunction. The FDA analysis found the capsules to contain sildenafil and acetaminophen.

June 17, 2024

Do Not Consume Diamond Shruumz Products, Warns CDC and FDA

On June 12, 2024, the Center for Disease Control and Prevention (CDC), Food and Drug Administration (FDA), and America’s Poison Centers warned consumers not to buy or consume Diamond Shruumz chocolate bars, cones, and gummies.

January 18, 2024

FDA Warns Consumers Not to Use Neptune’s Fix Products

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

December 19, 2024

Gout and Arthritis Supplement Recalled Due to Undeclared Drugs

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

March 01, 2023

Seller of Dr. Miller’s Herbal “Detox” Teas Warned by FDA for Drug Claims

On February 3, 2023, the FDA issued a warning letter to Jackson Health & Wellness Clinic after inspection of the company’s website found statements about the company’s Dr. Miller’s Holy Tea, Dr. Miller’s Super Holy Tea, Dr. Miller’s Ultimate Tea, Dr.

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). 

January 11, 2012

Herbal Extract Company Warned by FDA of Making Drug Claims

On January 3, 2012, the U.S. FDA sent a Warning Letter to Herbal Extract Plus, LLC regarding legal violations for claiming its herbal products can cure or prevent diseases.

March 02, 2022

Seller of Holistic Tea Warned by FDA

On February 17, 2022, the FDA issued a warning letter to Vital Health & Wellness following an inspection of the company’s website, which found statements made about the company’s product, Dr. Miller’s Holistic Premium Holy Tea, to be drug claims.

March 09, 2022

Court Bars Salud Natural From Selling Aloe, Joint Supplements & More

On March 8, 2022, a federal court ordered Salud Natural Entrepreneur, Inc. to stop distributing nutritional supplements that violate the Federal Food, Drug and Cosmetic Act (FDCA).

February 02, 2021

FDA Warns Seller of Reishi Mushroom Supplements

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

April 30, 2021

FDA Warns Seller of Fish Oil, Apple Cider Vinegar, Collagen, and Elderberry Supplements

On April 13, 2021, the FDA issued a warning letter to Orphic Nutrition following a review of the company's websites, which found statements made about the products Apple Cider Vinegar Capsules, Ashwagandha Capsules, Garcinia Cambogia Capsules, Premium Collagen Peptides Capsules, Elderberry ...

May 11, 2022

FDA Warns 10 Companies for Selling Workout Supplements With Dangerous Ingredients

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

December 22, 2021

FDA Warns Seller of Liquid Magnesium, B-12, Berberine & More

On December 9, 2021, the FDA issued a warning letter to Wholly Liquid Nutritional Supplements LLC because it found statements on the company's website and social media about its products, including SpiroLaze, BioLaze, LiquiLaurin, VIT-B12, DeStress, and Omega Plus, to be ...

December 15, 2020

FDA Warns Seller of Evening Primrose Oil and Beta Glucan

On December 2, 2020, the FDA issued a warning letter to Smoky Mountain Naturals, LLC following a review of the company's website, which found statements made about the company's products Evening Primrose Oil and Beta Glucan to be drug claims.

November 24, 2020

Recalled Vitamin D Contains Potentially Dangerous Ingredient

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

May 30, 2014

Seller of Brain, Diabetes, Echinacea Supplements and More Warned for Drug Claims

On April 22, 2014, the FDA issued a warning letter to Mundo Natural Inc., following a review of the company's website which found statements made about supplements Neuro AD, Stop Diabetes, Stop High Blood Pressure, Morninga 7 and Purpurea Echinacea to be drug claims.

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.

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 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.

November 24, 2018

Dangerous Drug In Supplements for Pain and Anxiety

On November 20, 2018, the FDA announced it has issued warning letters to two companies for the illegal marketing of products labeled as dietary supplements that contain the opioid-like drug tianeptine.

September 13, 2010

Supplement for "Increasing Desire" Recalled for Containing Drug

The U.S. FDA posted a notice regarding the recall of Masxtreme Capsules by the distributor, Natural Wellness, Inc. FDA analysis has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil.

July 20, 2010

Recall of ED Supplement Containing Drug

On July 20, 2010, the U.S. FDA posted a news announcement from Good Health, Inc. regarding the recall of Vialipro, a sexual enhancement supplement sold nationally.

April 08, 2010

Capsule for Men Spiked with Erectile Drug

On April 7, 2010, the U.S.

July 23, 2009

Six Male Enhancement Supplements Found Adulterated

On July 15, 2009, the U.S. FDA announced that Obteron 1 Inc. dba Nature & Health Co. is recalling the following supplements: LibieXtreme, Y-4ever, Libimax X Liquid, Powermania Capsule, Powermania Liquid, and Herbal Disiac.

April 21, 2012

FDA Finds Prescription Drug Analog in 3 Enhancement Supplements

On April 20, 2012, the U.S. FDA advised consumers not to purchase or use the following supplements from Enhance Nutraceutical: "Instant Hard Rod," "RigiRx Plus," and "Zen Maxx." FDA laboratory analysis confirmed that each contains aminotadalafil.

April 03, 2012

"France T253" Enhancement Supplement Contains Hidden Drug

April 3, 2012: The U.S. Food and Drug Administration (FDA) is advising consumers not to purchase or use “France T253,” a product for sexual enhancement. This product is promoted and sold on various Web sites, such as ebay.com.

May 17, 2012

FDA Warns of Drug Ingredients in Three Sexual Enhancement Supplements

On May 16, 2012, the U.S. FDA advised consumers not to purchase or use the following three sexual enhancement products: Boost - Ultra Sexual Enhancement Formula (sold on www.boostultra.biz), Firminite (sold on www.firminite.com), and VMaxx Rx (sold on www.vmaxxrx.com).

July 13, 2012

Alistrol Health Inc. Warned Over Health Claims on Products

On June 26, 2012, the FDA issued a warning letter to Alistrol Health Inc. for making product statements on the company's websites that constitute drug claims.

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.

April 07, 2011

Prostate Drug Found in Prostate Supplement -- Recall Underway

On March 24, 2011 the U.S. FDA posted a voluntary recall notice for U-Prosta from USA Far Ocean Group, Inc.

August 30, 2006

FDA Warns that Dietary Supplements Containing Ephedrine Alkaloids are Illegal and Pose Risk to Users

On August 21, 2006 the US Food and Drug Administration (FDA) issued a statement on the Tenth Circuit’s ruling to uphold the FDA decision banning dietary supplements containing ephedrine alkaloids.

September 12, 2018

FDA Urges Consumers to Avoid Kratom

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

March 30, 2019

FDA Warns Seller of Reishi, Joint Supplements, Ginseng & More for Pesticides, Other Violations

On March 12, 2019, the FDA issued a warning letter to Yanqing "Michael" Li and Chang Su, owners of the website http://www.woohoonatural.

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.

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.

March 08, 2012

Rx Drugs Found in Weight Loss and Enhancement Supplements

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

December 13, 2016

Case of Hemorrhagic Stroke Linked to Redline Energy Drink

A case of hemorrhagic stroke has been linked to the consumption of a single energy drink, according to a report published on October 11, 2016, in The American Journal of Emergency Medicine.

August 01, 2017

"Man of Steel" Sexual Enhancement Supplements Recalled

On July 27, 2017, Man of Steel recalled its Man of Steel 1 and Man of Steel 2 sexual enhancement supplements because they were found to contain undeclared sildenafil. 

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 02, 2012

Recall of Enhancement Supplement for Men -- Contains Drug

On Feb, 24, 2012, Regeneca, Inc. announced a voluntary nationwide recall of all lots of RegenErect. The product was distributed throughout the U.S. and Puerto Rico to Internet consumers. The product is distributed as a blue capsule sold individually in foil packets with a UPC code of 816860010055.

January 01, 2011

Recall of Two Supplements Spiked with Erectile Dysfunction Drug

On December 22, 2010 the U.S.

July 19, 2011

Recall of Enhancement Supplement for Men - Contains Drug Compounds

On July 13, 2011, Global Wellness, LLC announced an expanded voluntary nationwide recall of Via Extreme Ultimate Sexual Enhancer Dietary Supplement for Men. The product was distributed throughout the U.S. Puerto Rico, Barbados, and Canada to internet and retail consumers.

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 14, 2009

Nationwide Recall of Sexual Enhancement Supplements Containing Drug-like Compound

On December 14, 2009, the Federal Drug Administration (FDA) posted a notice on its website regarding the recall of many sexual enhancement supplements sold by Atlas Operations, Inc.

September 12, 2010

Mr. Magic Male Enhancer Recalled

The U.S. FDA posted a recall announcement daated August 18, 2010 from Glow Industries regarding "Mr. Magic Male Enhancer from Don Wands.

August 13, 2010

Recall of Male Enhancement Supplement Sold in National Stores

On August 9, 2010 the U.S. FDA announced that the company Prolatis' of Salt Lake City, Utah is conducting a voluntary recall of the company's product sold as Prolatis'.

November 26, 2007

Encore Tabs Recalled -- Contain Prescription Drug

On November 21, 2007, Bodee LLC announced today that it is conducting a voluntary nationwide recall of all the company's supplement product sold under the name Encore Tabs.

July 30, 2008

Recall of Viapro Capsules Due to Potentially Harmful Ingredient

The U.S. FDA has posted a release noting that EG Labs, LLC announced a nationwide voluntary recall on July 23, 2008 of all lots of its supplement product sold under the brand name, Viapro, in 375mg capsules.

May 29, 2008

Recall of Virility Supplement

On May 29, 2008, the FDA posted a recall by International Pharmaceuticals, Ltd. of all of the company's supplement sold under the name of Viril-Ity-Power (VIP) Tabs, 560mg/serving.

February 16, 2012

Recall of Enhancement Supplement for Women -- Contains Drug

On Feb, 10, 2012, Regeneca, Inc. announced a voluntary nationwide recall of RegenArouse Natural Female Intimacy Enhancement. The product was distributed throughout the U.S. and Puerto Rico to Internet consumers. The product is distributed as a pink capsule sold individually in foil packets.

March 04, 2008

Two Supplements Recalled for Containing Viagra-like Compounds

On March 4, 2008, the FDA posted a release from Palo Alto Labs (dated February 28) announcing a voluntary nationwide recall of the company's supplement products sold under the name Aspire36 and Aspire Lite.

March 20, 2007

Recall of Adulterated Sexual Enhancement Supplement

As posted on the FDA website, on March 15, 2007, the company Barodon SF of Los Angeles, CA announced that it is conducting a voluntary nationwide recall of the company's supplement product sold under the name V.MAX.

November 03, 2004

FDA Warns of Sexual Enhancement Supplements Containing Prescription Drug

On November 2, 2004, the Food and Drug Administration (FDA)warned consumers not to purchase or to consume Actra-Rx or Yilishen, two products promoted and offered for sale on Web sites as "dietary supplements" for treating erectile dysfunction and enhancing sexual performance for men.

June 23, 2003

FDA Warns Consumers Against Taking 6 Sexual Enhancement Supplements

On June 20, 2003, the Food and Drug Administration (FDA) warned consumers not to purchase or consume the following products: SIGRA, STAMINA Rx and STAMINA Rx for Women, Y-Y, Spontane ES and Uroprin, manufactured by NVE, Inc., in Newton, N.J. and distributed by Hi-Tech in Norcross, Ga.

September 18, 2012

Maker of Noni, Nopal, Blood Sugar and Cholesterol Supplements Warned For Drug Claims, Misbranding, and Manufacturing Violations

On August 27, 2012, the FDA issued a warning letter to Naturavit, Inc. for making statements about dietary supplements Noni Imperial Hawaiian, Garlic and Parsley, Cholestol, Nopal and Diatrin that constitute drug claims.

February 24, 2025

Vitality Sexual Enhancement Supplement Recalled

On February 20, 2025, One Source Nutrition recalled all lots of Vitality capsules after FDA analysis found the supplements to contain undeclared prescription drugs sildenafil and tadalafil, which are not permitted in dietary supplements.

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.

October 21, 2014

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

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

November 02, 2012

Maker of Joint Health, Blood Sugar, Prostate, Ginkgo Supplements and More Warned For Drug Claims, Misbranding and Adulteration

On September 10, 2012, the FDA issued a warning letter to Global Source Management & Consulting for making drug claims about the following dietary supplements: Scientific Joint Program capsules, Alpha Lipoic Acid, Healthy Blood Sugar Diabetic Support, Dr.

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.

March 25, 2008

FDA Warns of Sexual Supplements with Drug-like Ingredients

On March 25, 2008, the U.S. Food and Drug Administration advised consumers not to purchase or use "Blue Steel" or "Hero" products marketed as dietary supplements throughout the United States because they are considered unapproved drugs and have not been proven to be safe or effective.

May 10, 2007

FDA Warns of Two Supplements Containing Pharmaceutical-like Compounds

On May 10, 2007, the FDA advised consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States.

October 30, 2008

Possible Risk Rather than Benefit Found in Trial of Vitamin E and Selenium for Prostate Cancer

On October 27, 2008 the National Cancer Institute (NCI) announced that men in the Selenium and Vitamin E Cancer Prevention Trial (SELECT) are being told to stop taking their supplements.

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.  

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 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.

November 16, 2023

Toxic Levels of Lead Found in Cinnamon Applesauce

WanaBana, Schnucks, and Weis apple cinnamon fruit puree pouches have been recalled after being linked, as of December 5, 2023, to 64 reports of illness, including four children with potential lead toxicity.

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 ...

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 ...

August 30, 2012

Supplement Company Warned For Medical Claims and Misbranding Of Omega-3, CoQ10, Noni Juice And More

On July 12, 2012, the FDA issued a warning letter to Alfa Vitamins Laboratories, Inc.

June 15, 2009

Sexual Enhancement Supplement Recalled -- Second Time Found with Drug-like Compound

On June 15, 2009, the U.S. FDA announced that, per its order, Hi-Tech Pharmaceuticals, Inc. is conducting a nationwide voluntary recall of the company's product sold under the name Stamina-Rx.

April 19, 2007

Recall of Another Sex Enhancement Supplement

On April 17, 2007 the Food and Drug Administration (FDA) website posted an announcement that Jen-On Herbal Science International, Inc. is conducting a voluntary nationwide recall of the company's supplement product sold under the name H S Joy of Love. Jen-On Herbal Science International, Inc.

December 30, 2007

FDA Warns Consumers Not to Use Several "Shangai" Sexual Enhancement Supplements

On December 28, 2007, the U.S. Food and Drug Administration (FDA) advised consumers not to buy or use Super Shangai, Strong Testis, Shangai Ultra, Shangai Ultra X, Lady Shangai, and Shangai Regular, also marketed as Shangai Chaojimengnan, products.

July 29, 2008

Recall of Sexual Enhancement Supplements Containing Drug

On July 28, 2008 the U.S. FDA announced that Jack Distribution, LLC and G & N works, Inc. are conducting a voluntary nationwide recall of all lot numbers of the company's supplement products sold under the brand names Rize 2 The Occasion and Rose 4 Her.

October 10, 2003

Government Stops Sale of Supplements Claiming to Treat Obesity and Impotence

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

March 17, 2025

Zaarah Herbal Powders Recalled Due to Lead, Arsenic Risk

On March 10, 2025, New York Wholesale Group recalled Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka Powder and Zaarah Herbals Bhringraj Powder because they have the potential to be contaminated with elevated levels of lead and arsenic.

January 30, 2013

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

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

August 08, 2014

FDA Warns Puerto Rico Supplement Seller

On June 30, 2014, the FDA issued a warning letter to Mr. Ramon Rosa, following a review of his website, www.aceitedeguanabana.

February 07, 2013

Growth Factor Supplement For "Size, Strength and Stamina" Recalled Due To Potential Contamination

On January 2, 2013, EonNutra, LLC issued a voluntary recall of specific batches of Soto Supplements Growth Factor Complex 200 GFC 200 (2 fl oz.) liquid dietary supplement due to potential bacterial contamination.

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.

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. 

September 07, 2016

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

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

November 06, 2014

Seller of Cholesterol, Arthritis Supplements and More Warned for Drug Claims

On October 17, 2014, the FDA issued a warning letter to Vitamins Direct (USA) and Golden Pride, Inc., which distribute Flexezy and Physician's Signature brands of dietary supplements, following a facility inspection which found statements made about certain supplements to be drug claims.

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.

November 21, 2022

6 Supplement Companies Warned by FDA for Making Cholesterol Claims

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

February 13, 2013

Manufacturer of Heart, Multivitamin, Cranberry, and Longevity Supplements Warned For Adulteration and Drug Claims

On January 29, 2013, the FDA issued a warning letter to M.D.R. Fitness Corp. following a facility inspection which found violations of good manufacturing practices which cause the company's products to be adulterated. 

May 28, 2008

FDA Requests Recall of Xiadafil VIP Supplements

On May 27, 2008, the U.S. The U.S. Food and Drug Administration announced that it had requested that SEI Pharmaceuticals, of Miami, Fla.

July 13, 2006

FDA Warns About Sexual Enhancement Supplements with Dangerous Ingredients

On July 12, 2006, the Federal Drug Administration (FDA) warned consumers not to purchase or consume Zimaxx, Libidus, Neophase, Nasutra, Vigor-25, Actra-Rx, or 4EVERON.

August 03, 2023

Arsenic Poisoning in U.S. from Ayurvedic Supplements

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

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.

August 17, 2021

Weight Loss Supplements Found to Contain Sibutramine Recalled

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

December 22, 2008

FDA Warns Consumers About Tainted Weight Loss Pills

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

October 02, 2023

Dangerous Ingredients Found in Ten Arthritis and Pain Supplements

On September 29, 2023, the FDA warned consumers that the following arthritis and pain management products contain undeclared drugs such as diclofenac, methocarbamol (a muscle relaxant), and dexamethasone (a corticosteroid), and/or other potentially harmful ingredients.

October 26, 2023

Joint Pain Supplements Recalled Due to Undeclared Drug Ingredients

On October 22, 2023, Botanical-Be recalled of all lots of the company’s Kuka Flex Forte, Artri King, and Reumo Flex capsule products after FDA laboratory analysis found them to contain undeclared diclofenac.

August 12, 2024

FDA Warns "Apricot Power" Apricot Seeds Contain Toxic Compound

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

October 08, 2024

AK Forte Joint Pain Supplement Recalled

On October 8, 2024, C&A Naturistics voluntarily recalled all lots of AK Forte, 400 mg tablets because FDA laboratory analysis found products to contain undeclared diclofenac, dexamethasone, and methocarbamol.

August 20, 2024

Two Sexual Enhancement Supplements Sold on Amazon Recalled

On August 20, 2024, Veata LLC Endurance Pro Energy Boost capsules and Boulla LLC Boom Max capsules were recalled because they contain sildenafil, a prescription medication which is not permitted in dietary supplements.

January 28, 2025

Shatavari Powder Recalled Due to Risk of Lead Contamination

On January 27, 2025, New York Wholesale Group recalled Zaarah Herbals shatavari powder because of potential lead contamination.

February 27, 2025

Male Enhancement Supplement Sold on Amazon and Walmart Recalled

On February 25, 2025, Natural Dior LLC recalled affected lots of a dietary supplement Vitafer-L Gold Liquid because it contains undeclared tadalafil, which is not permitted in dietary supplements.

February 03, 2025

Four Male Enhancement and Energy Supplements Found to Contain Drugs

On January 16, 2025, the FDA issued a Warning Letter to Mihon Corp. d/b/a VitalityVita and Boulla, LLC after FDA analysis found four of the company’s supplements, VitalityXtra, PeakMax, ZapMax, and ZoomMax, to contain undeclared sildenafil.

February 05, 2025

Muscle Tech Alpha Test Recalled

On December 18, 2024, Iovate Health Sciences USA Inc. recalled 10 lots (163,248 units) of Muscle Tech Alpha Test capsules because they contain cathine, a controlled substance that can cause serious adverse effects.

April 23, 2025

FDA Warns Consumers Not to Use ADVANCED KING Joint Supplement

On February 10, 2025, the FDA warned consumers not to purchase or use the joint pain supplement ADVANCED KING (Naturista Store LLC), because FDA analysis confirmed the product contains dexamethasone, diclofenac, and methocarbamol.

May 01, 2025

Male Enhancement Supplements Recalled

On April 25, 2025, Health Fixer recalled all lots of Male Ultra, Malextra, Electro Buzz, Ultra Armor and Male Ultra Pro supplements because laboratory analysis found them to contain chloropretadalafil, propoxyphenylsildenafil, and sildenafil, drugs that are not permitted to be ...

May 08, 2025

Male Endurance Supplement Sold on Amazon Recalled

On May 6, 2025, EnShiShiXiangNiShangMaoYouXianGongSi recalled one lot of Endurance Boost With Horny Goat Weed capsules because they were found to contain sildenafil and propoxyphenylsildenafil (a sildenafil analogue), drugs that are not permitted in dietary supplements.

May 08, 2024

APG SEVEN Warned for Promoting Products for Cancer, Depression, Arthritis, & More

On April 18, 2024, the FDA issued a Warning Letter to APG SEVEN, INC following a review of the company’s product labels, website, and social media, which found statements about the company’s BioMoringa, BioDiabetin, Maca Plus, BioProstate, Immune Support, HongoTrap, Honbacterol, ...

August 11, 2022

Problems With Supplements on Amazon

More than 50% of 30 top-listed immune support supplements purchased on Amazon.com in May of last year were found to list ingredients that could not be found in them with testing, according to a recent report (Crawford, JAMA Network Open, 2022).

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.

January 19, 2023

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

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

July 13, 2023

1st phorm Level-1 Protein Supplements Recalled Due to Staph Risk

On June 21, 2023, International Food Companies DBA International Food Products recalled two protein supplements due to potential contamination with Staphylococcus aureus.

July 26, 2023

Gadget Island, Inc. Male Enhancement Supplements Found to Contain Prescription Drugs

On July 21, 2023, the FDA issued a warning letter to Gadget Island, Inc.

August 25, 2023

FDA Warns Consumers Not to Use Big Guys Male Energy Supplement

On August 22, 2023, the FDA warned consumers not to buy or use BIG GUYS Male Energy Supplement after FDA laboratory analysis found it to contain undeclared sildenafil.

September 06, 2023

WEFUN Capsules Recalled Due to Undeclared Sildenafil

On August 25, 2023, WEFUN Inc. issued a recall of 300 boxes of WEFUN Capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

February 07, 2024

Sustain and Schwinnng Male Enhancement Supplements Recalled

On February 2, 2024, Today the World issued a recall of all lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules after FDA analysis found the supplements to contain undeclared prescription drugs tadalafil and nortadalafil.

January 03, 2024

FDA Warns Amazon for Selling Men’s Supplements Containing Prescription Drugs

On December 20, 2023, the FDA issued a Warning Letter to Amazon.com, Inc.

November 30, 2023

Original The Rock Capsules Recalled Due to Undeclared Sildenafil

On October 18, 2023, Noah’s Wholesale, LLC issued a nationwide recall of one lot of the company’s Original The Rock capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

March 21, 2024

Eleven Brands of Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs

On March 19, 2024, Pyramid Wholesale issued a recall of 11 brands of sexual enhancement supplements, including honey-based products, after they were found to contain undeclared sildenafil and tadalafil.

April 03, 2024

ForeverMen Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs

On February 12, 2024, ForeverMen issued a recall of all lots of ForeverMen capsules, which are promoted for sexual enhancement, after FDA analysis found the capsules to contain undeclared sildenafil and tadalafil.

May 01, 2024

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

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

June 12, 2024

Integrity Enhancement Supplements for Men Recalled Due to Undeclared Prescription Drugs

On February 1, 2024, Integrity Products issued a recall of one lot of Ram It & To The Moon products, which are promoted for sexual enhancement, after FDA analysis found the capsules to contain undeclared sildenafil and tadalafil.

November 07, 2024

Sexual Enhancement Supplements Sold on Amazon Recalled

On November 4, 2024, four sexual enhancement supplements sold on Amazon and other websites, ZoomMax and ZapMax (Boulla LLC) and VitalityXtra and PeakMax (VitalityVita LLC) were recalled because they were found to contain undeclared prescription drugs, ...

February 28, 2024

Microbial Contamination Found in LightEyez MSM Eye Drops

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

April 27, 2022

Prescription Drugs Found in Arthritis, Muscle Pain, and Osteoporosis Supplements

On April 20th, 2022, the FDA warned consumers not to use the following ”Artri“ or ”Ortiga” products promoted to treat arthritis, muscle pain, osteoporosis and bone cancer because they have been found to contain undeclared drugs that can have serious adverse ...

February 25, 2022

Similac, Other Infant Formulas Recalled, Linked to Illness and One Death

Update: (3/7/22) This recall has been expanded to include one lot of Similac PM 60/40 following the death of an infant who tested positive for Cronobacter sakazaki and consumed Similac PM ...

July 15, 2022

Honey-Based Enhancement Supplement Recalled

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

July 01, 2022

Male Enhancement Supplements Sold on Amazon Recalled

On January 27, 2022, Loud Muscle Science LLC issued a voluntary recall of various lots of Launch Sequence supplements because they were found to contain the prescription drug tadalfil.

July 13, 2022

FDA Warns Sellers of Tainted Honey-Based Sexual Enhancement Products

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

August 03, 2022

Sexual Enhancement Supplement Recalled Due to Sildenafil

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

July 26, 2022

Sexual Enhancement Supplement Sold on Amazon Recalled

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

February 13, 2023

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

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

January 11, 2023

Male Sexual Enhancement Supplement Found to Contain Prescription Drug

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

September 29, 2022

Sexual Enhancement Supplement Sold on Amazon and Walmart Recalled Due to Undeclared Drugs

On September 27, 2022, Proper Trade LLC/My Stellar Lifestyle recalled two lots of Wonder Pill after Amazon laboratory analysis found the product to contain undeclared tadalafil, a prescription medication.

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.

November 17, 2022

FDA Warns Consumers Not to Use Male Enhancement Supplement

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

June 14, 2023

Havasu Beet Root Powder Recalled Due to Allergen Risk

On June 12, 2023, Supplement Manufacturing Partner Inc. issued a recall of one lot of Havasu Nutrition’s Beet Root Powder + due to undeclared milk. The recall was initiated following a report of an allergic reaction from a consumer with a milk allergy.

May 04, 2023

PrimeZEN Enhancement Supplement for Men Found to Contain Prescription Drug

On April 27, 2023, the FDA issued a warning letter to Tager Online, Inc. DBA Volt Candy; Volt Candy Wholesale Club after FDA laboratory analysis determined PrimeZEN Black 6000, a product promoted to improve sexual function for men, contains tadalafil and sildenafil.

September 14, 2023

Toxic Herb Found In Weight Supplements

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

June 20, 2003

FTC Charges Marketers of Seasilver with False and Deceptive Claims

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

December 08, 2011

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

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

April 21, 2020

Life Force Warned for Colloidal Silver, Nitric Oxide Claims

On March 27, 2020, the FDA issued a warning letter to Doctor's Signature Sales and Marketing International Corp.

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.

October 01, 2019

Lead and Arsenic Found in Multi Mineral & Vitamin Supplement

On September 30, 2019, Cellect Products Inc. and Oglethorpe Ltd. issued a recall of one lot of Cellect®, Essentials Factor® Multi Mineral & Vitamin Supplement Unflavored Powder Mix because it was found to contain unsafe levels of lead and arsenic.

June 02, 2022

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

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

July 10, 2020

Sundial Herbal Recalls More Than Sixty Products Including Turmeric, Cinnamon & Tea

On July 9, 2020, Sundial Herbal Products issued a recall of more than 60 herbal products because they were misbranded and/ or promoted with drug claims. Their labels contain drug claims stating the products can diagnose, cure, mitigate, treat, or prevent disease.

June 30, 2020

FDA Warns Seller of Alpha Lipoic Acid, Berberine, and More

On June 18, 2020, the FDA issued a warning letter to Only Natural, Inc. dba Bio Nutrition, Inc.

July 27, 2021

"Miss Slim" Capsules Recalled

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

July 20, 2021

Alpha Male Plus Recalled

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

November 05, 2021

Herb Recalled Due to Risk of Lead, Cadmium Contamination

On November 2, 2021, Murray Int'l Trading issued a recall of Herbal Doctor brand Angelicae Sinensis due to potential risk it may contain elevated levels of lead and cadmium.

February 10, 2022

Three Sexual Enhancement Supplements Sold on Amazon Recalled

On February 8, 2022, specific lots of three male sexual enhancement supplements, Red Mammoth capsules, MAC DADDY RED capsules, MAC DADDY PURPLE capsules, and The Red Pill capsules, were recalled because Amazon laboratory analyses found them to contain undeclared ...

April 05, 2022

Sexual Enhancement Capsules for Men Recalled

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

August 01, 2022

53 Protein, Meal Replacement and Nutritional Beverages Recalled Due to Bacterial Contamination

On July 29, 2022, Lyons Magnus LLC issued a recall of 53 protein, meal replacement, and nutritional beverages, including those sold under the brand names of Glucerna, Premier Protein, Oatly, and others, due to the potential for microbial contamination, including from Cronobacter sakazakii.

June 22, 2023

FDA Warns Warrior Labz for Selling Products with Steroid-Like Substances and Prescription Drugs

On June 12, 2023, the FDA issued a warning letter to Warrior Labz SARMS following inspection of the company’s website and social media, which found that the company sold the following products labeled as containing steroid-like substances known as selective androgen receptor modulators ...

October 11, 2023

Family Sentenced to Over 12 Years in Prison for Selling Dangerous “Bleach” Miracle Mineral Solution as “COVID Cure”

Four Florida men who distributed the toxic bleach solution Miracle Mineral Solution (MMS) as a cure for COVID-19 and other serious medical conditions have been sentenced to 5 to 12 years in prison for conspiring to defraud the United States.

May 04, 2019

High Levels of Lead Found in Chinese Herbal Supplements

On May 2, 2019, Life Rising Corporation issued a recall Life Rising Holder-W Holder Warmer capsules, Life Rising NECK-ND Neck Clear capsules, and HoliCare Metabolism Cleansing (MET-CLS) tablets after FDA testing found high levels of lead in samples of the products.

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 ...

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.

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.

February 17, 2021

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

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

September 03, 2020

Red-E Male Enhancement Capsule Recalled

On September 1, 2020, The Protein Shoppe, LLC issued a recall of Red-E male enhancement capsules because FDA analysis found it to contain sildenafil.

April 26, 2021

Family Indicted for Selling Dangerous "Bleach" Miracle Mineral Solution As "COVID" Cure

Four Florida men have been indicted by a Miami federal grand jury on charges of fraudulently marketing and selling the toxic bleach solution Miracle Mineral Solution (MMS) as a cure for COVID-19 and other serious medical conditions, such as cancer, Alzheimer's, diabetes, autism, malaria, ...

April 17, 2021

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

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

April 10, 2021

Three More Male Enhancement Products Recalled Due to Undeclared Drugs

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

April 02, 2021

Three Male Enhancement Products Recalled Due to Undeclared Drugs

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

December 15, 2020

FDA Warns JC Ayur Life LLC for Drug Claims

On October 29, 2020, the FDA issued a warning letter to JC Ayur Life LLC following a review of the company's website, which found statements made about the company's product Heritage of Ayurveda Dia-Tonic Incudil Herbal Dietary Supplement to be drug claims.

January 17, 2018

Joint and Pain Relief Product Contains Undeclared Drug

On January 17, 2018 Health Canada warned consumers that Linsen Double Caulis Plus, a supplement for joint pain, was found to contain the undeclared drug dexamethasone.

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.

November 21, 2012

Maker of Blood Pressure, Probiotic, Resveratrol and Hormonal Supplements Warned For Manufacturing Violations and Drug Claims

On November 2, 2012, the FDA issued a warning letter to Atrium, Inc. following a facility inspection which found a number of the company's dietary supplements to be adulterated or promoted as drugs.

December 21, 2012

Dangerous Supplement Being Sold Under New Name

On December 21, 2012, the FDA warned consumers that Reumofan Plus, a dietary supplement promoted for arthritis and muscle pain that has been linked to serious and sometimes fatal side effects, is now being sold under the name WOW.

June 04, 2012

FDA Warning on Supplement for Pain Relief

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

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.

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:

March 17, 2020

"Active Male" Supplement Recalled

On March 16, 2020, Natural Remedy Store recalled all lots of Active Male, 500mg, to the consumer level because FDA analysis has found the product contains tadalafil.

November 16, 2019

Silver Bullet Supplement for Men Recalled

On November 13, 2019, Nature's Rx issued a recall of one lot of Silver Bullet male enhancement capsules because FDA analysis found it to contain sildenafil.

November 12, 2019

Libido Supplement for Men and Women Recalled

Update: (2/25/20) This recall has been expanded to include lots of an additional Med Man product, Bow and Arrow libido enhancer for men, highlighted below.

October 26, 2019

Green Lumber Enhancement Supplements Recalled

On October 22, 2019, GL Holdings issued a recall of Green Lumber, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain tadalafil.

September 21, 2019

Liquid Vitamin C for Men Recalled

On September 16, 2019, Fitoterapia USA Inc. issued a recall of Macho Artificial Passion Fruit Flavored Vitamin C Liquid Supplement, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain tadalafil.

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 23, 2019

FDA Warns Seller of CBD Lotions, Patches, Tinctures and Pet Products

On July 22, 2019, the FDA issued a warning letter to Curaleaf, Inc.

December 21, 2019

Men's Enhancement Supplement Recalled

On December 17, 2019, Motto International Corp all lots of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000, to the consumer leve because FDA analysis has found they contain tadalafil.

July 14, 2020

Sellers of Miracle Mineral Solution Criminally Charged With Making Coronavirus Claims

On July 8, 2020, federal prosecutors charged the sellers of Miracle Mineral Solution, a toxic bleach solution marketed as a cure for coronavirus (COVID-19), with conspiracy to defraud the United States, conspiracy to violate the Federal Food, Drug and Cosmetic Act, and criminal contempt.

March 26, 2021

Nine Banned Stimulants Found in Workout, Weight Loss Supplements

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

November 28, 2015

Herbal Supplements Linked to Heavy Metal Poisoning

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

September 18, 2015

High Levels of Mercury and Lead Found in Ayurvedic Herbal Supplements

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

August 30, 2012

FDA Warns of Medical Claims Made For Numerous Chinese Herbal Products

On August 15, 2012, the FDA warned Dragon Herbs that promotional statements made on the company's website constitute drug claims for twenty herbal products, including CardioPro 2000, Cordyceps, Duanwood Reishi, Gynostemma, Ginseng and Astragalus Combination, Dang Gui and Gelatin, Sweet Relief, ...

October 24, 2015

Eight Enhancement Supplements Found to Contain Undeclared Drugs

On October 23, 2015, the FDA warned consumers not to buy or use the following three sexual enhancement supplements because they were found to contain an undeclared sildenafil or similar drugs (some were identified during an examination of international mail shipments): 

April 17, 2015

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

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

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.

November 14, 2014

FDA Warns Consumers Not to Buy or Use Muscle Enhancement Supplement

On November 13, 2014, the FDA advised consumers not to buy or use the muscle enhancement supplement Mayhem (Chaotic-Labz) because it was found to contain the undeclared drugs cyproheptadine and dexamethasone. These drugs can cause serious side effects and can interact with other medications.

February 20, 2013

Recall: Arthritis and Muscle Pain Supplement Contains Prescription Drugs

On February 15, 2013, Reumofan Plus USA, LLC and Reumofan USA, LLC announced a recall of Reumofan Plus, a dietary supplement promoted for arthritis and muscle pain, because it was found to contain the active pharmaceutical ingredients methocarbamol, dexamethasone, and diclofenac.

August 08, 2016

Turmeric Spice Recall Expanded to Include More Brands

On August 5, 2016, Gel Spice, Inc. expanded its recall of one lot of Fresh Finds Ground Turmeric Powder to include other turmeric spices sold under different brand names due to elevated levels of lead.

July 29, 2016

Ground Turmeric Spice Recalled Due to Lead Contamination

On July 28, 2016, Gel Spice, Inc. issued a voluntary recall one lot of Fresh Finds Ground Turmeric Powder because it was found to contain elevated levels of lead.

January 22, 2019

FDA Warns Consumers Not to Use "The Silver Bullet"

On January 10, 2019, the FDA warned consumers not to buy or use the sexual enhancement supplement The Silver Bullet because it contains undeclared sildenafil and tadalafil.

January 13, 2019

Sexual Enhancement Supplement Recalled

On January 8, 2019, Happy Together, Inc. issued a recall of the sexual enhancement supplement Rhino 5k because FDA analysis found it to contain undeclared sildenafil and tadalafil.

December 11, 2018

Sexual Enhancement Supplement Found to Contain Prescription Drug

On December 10, 2018, the FDA warned consumers that the sexual enhancement supplement On Demand contains undeclared sildenafil.

December 01, 2018

Sexual Enhancement Supplements Contain Prescription Drugs

The FDA recently warned consumers that the following sexual enhancement supplements were found to contain undeclared sildenafil and/or tadalafil. Use the links below to read the complete warning letter for each:

• Willy Go Wild

March 06, 2019

FDA Warns Consumers Not to Use Certain Sexual Enhancement Supplements

On January 28, 2019, the FDA warned consumers not to buy or use the following sexual enhancement supplements were found to contain undeclared sildenafil and/or tadalafil.

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.

December 14, 2010

FDA Warns Consumers to Avoid Man Up Now Capsules

On December 14, 2010, the U.S. FDA warned consumers not to use Man Up Now capsules, marketed as a dietary supplement for sexual enhancement, because they contain a variation of an active drug ingredient found in Viagra that can dangerously lower blood pressure.

November 11, 2015

Consuming a Single Energy Drink May Increase Cardiovascular Risk

A recently published study found that consumption of a single caffeinated energy drink significantly increased blood pressure and noradrenaline levels in healthy young adults. The researchers noted these changes could potentially increase the risk of cardiovascular events.

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.

July 29, 2017

Increase in Calls to Poison Control Centers About Supplements

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

August 05, 2017

Children's Ayurvedic Medicine Formula Contains High Levels of Lead

On August 4, 2017, the FDA warned parents and caregivers not to use Balguti Kesaria Ayurvedic Medicine due to the risk of lead poisoning. 

December 12, 2015

Sexual Enhancement Supplement Recalled

On December 11, 2015, Reesna Inc. issued a recall of its sexual enhancement supplements Fuel Up Plus and Fuel Up High Octane which were distributed in August 2015 and were found to contain undeclared hydroxythiohomosildenafil.

March 09, 2016

Four Sexual Enhancement Supplements Recalled

On March 7, 2016,  Health Canada (the Canadian equivalent of the FDA) announced that Vivo Brand Management is recalling four sexual enhancement products sold in Canada which may contain the undeclared drug sildenafil. Some of these products also appear to be available for purchase in the U.S.

August 31, 2016

Recall of Dangerous Chinese Herbal Supplement Expanded

On August 30, 2016, Ton Shen Health expanded its initial recall of DHZC-2 tablets to include all lots purchased before August 24, 2016, due to potential contamination with elevated levels of lead.

October 04, 2016

Turmeric Spice Recalled Due to Elevated Lead Levels

On September 26, 2016, Spices USA Inc. issued a recall of 772 bags of TASTY SAWA GROUND TURMERIC because it contains elevated levels of lead.

August 05, 2016

More Turmeric Spice Recalled

On August 5, 2016, JM Exotic Foods, Inc. issued a recall of ground turmeric because it was found to contain elevated levels of lead.

August 16, 2016

Chinese Herbal Supplement Recalled Due to Lead Contamination

On August 11, 2016, Ton Shen Health issued a recall its DHZC-2 tablets due to potential contamination with elevated levels of lead.

July 10, 2017

Bodybuilding Supplements Containing Steroid-Like Substances Recalled

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

November 29, 2016

Bentonite Clay Promoted for "Detoxification" Contaminated With Lead

On June 17, 2016, the FDA issued a warning letter to Best Bentonite, following a facility inspection and laboratory analysis of product sample which found the company's Best Bentonite to be contaminated with lead.

November 08, 2016

Chinese Herbal Supplement With Lead Contamination Recalled

On November 7, 2016, Ton Shen Health issued a recall its Life Rising brand of Side Head Regulator TT tablets because they were found to contain elevated levels of lead for children under the age of 18.

August 28, 2008

FDA Finds Fault with Generic Toprol XL -- Problems Reported Earlier by ConsumerLab.com

On August 12, 2008, the U.S. FDA sent a letter to Sandoz Inc. warning of violations in its manufacture of Metoprolol Succinate ER tablets and other drug products. Sandoz's Metoprolol Succinate ER tablets are generic versions of Toprol XL.

March 29, 2013

Prescription Drugs Found In Prostate and Sexual Enhancement Supplements

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

October 18, 2017

FDA Warns Seller of Arthritis, Blood Pressure, Diabetes Supplements For Making Drug Claims

On August 15, 2017, the FDA issued a warning letter to Years to Your Health, Inc., following an inspection of the company's website which found a number of their products to be misbranded, as they contained drug claims.

September 19, 2018

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

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

August 22, 2012

FDA Warns of Life-Threatening Side Effects and Withdrawal Symptoms from Two Arthritis, Muscle Pain Supplements

On August 21, 2012, the FDA issued a warning to consumers about the dangers of taking Reumofan Plus and Reumofan Plus Premium, two dietary supplements marketed for arthritis, osteoporosis and muscle pain.

September 13, 2014

Three Weight Loss Supplements Found to Contain Drugs

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

February 26, 2015

Weight Loss Supplement Found to Contain Multiple Drugs

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

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:

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.

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.

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.

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.

February 02, 2018

Seller of Vitamin D, Omega-3's, Whey Protein & More Warned for Drug Claims

On January 24, 2018 the FDA issued a warning letter to Young Health Products, LLC following a review of the company's website which found promotional statements and testimonials made about the certain products, including Lugol's Solution 2%, Liquid Vitamin D3, Probimune, Flax Seed & Omega ...

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 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.

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:

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.

November 06, 2009

FDA Warns that "Stiff Nights" Enhancement Supplement Contains Undeclared Drug

On November 5, 2009 the U.S. Food and Drug Administration (FDA) warned consumers that Stiff Nights, a product marketed as a dietary supplement for sexual enhancement, contains an ingredient that can dangerously lower blood pressure and is illegal.

August 01, 2013

Fat Loss and Muscle Enhancement Supplements Found To Contain DMAA

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

September 19, 2018

FDA Warns Seller of Shilajit

On September 6, 2018, the FDA issued a warning letter to Adaptive Energy LLC, following an inspection of the company's website, which found statements made about its shilajit product, Purblack were found to be drug claims.

September 04, 2018

Federal Court Shuts Down Maker of Sexual Enhancement Products

On August 30, 2018, the FDA announced that U.S.

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.

March 26, 2019

LEOPARD Miracle Honey Recalled

On March 22, 2019, USA LESS issued a recall of all lots of LEOPARD Miracle Honey, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.

March 23, 2019

BLUEFUSION Capsules for Sexual Enhancement Recalled

On March 21, 2019, Ata Int. Inc. issued a recall of its BLUEFUSION capsules, which are promoted for sexual enhancement, because FDA analysis found them to contain sildenafil, tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin and daidzein.

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.

May 15, 2019

Titanium 4000 Capsules for Men Recalled

On May 7, 2019, D.B.P. Distribution issued a recall of Titanium 4000, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil and tadalafil.

May 07, 2019

"The Beast" Supplement for Men Recalled

On May 7, 2019, STIFF BOY LLC issued a recall of The Beast, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.

April 12, 2019

Sexual Enhancement Supplement for Men Recalled

On April 9, 2019, SD Import, LLC issued a recall of Aphrodisiac, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.

April 08, 2019

Herbal "Coffee" for Sexual Enhancement Recalled

On March 22, 2019, Brian Richardson DBA "In Tha Pink" issued a recall of  ground Kopi Jantan Tradisional [sic] Natural Herbs Coffee, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil and tadalafil.

November 25, 2007

Recall of Men's "Sexual Energy" Supplement Expanded to Include "Energy Max" Product

On November 16, 2007, American True Man Health Incorporated announced that it is expanding it's voluntary recall of the Company's dietary supplement product sold under the name and identified as True Man's Sexual Energy Nutriment Men's Formula with the expiration date up to and including December ...

June 22, 2011

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

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

April 04, 2013

Three More Sexual Enhancement Supplements Found To Contain Undeclared Drugs

On April 3, 2013, the FDA warned consumers that the sexual enhancement supplements AFFIRM XL, Love Rider and Ninja Mojo were found to contain undeclared erectile dysfunction drugs. Consumers are urged to stop using these supplements immediately.

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:

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.

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 ...

August 15, 2017

Protein Supplements Can Be Dangerous in People with Rare Genetic Disorder

It was recently reported by Yahoo Australian News (August 14, 2017) that a 25-year-old woman died after taking protein supplements and eating protein-rich foods such as lean meats and egg whites in preparation for a fitness competition.

September 23, 2017

Enhancement Supplement "Vegetable Vigra" Recalled

On September 20, 2017, Gadget Island, Inc. Dba Gear Isle recalled VEGETABLE VIGRA [sic] after FDA testing found undeclared presence of sildenafil. 

September 21, 2017

Sexual Enhancement Supplements Containing Prescription Drugs Recalled

On September 20, 2017, Gadget Island, Inc. Dba Gear Isle recalled the following supplements because they were found to contain undeclared sildenafil and tadalafil:

• Rhino 7 Platinum 5000 capsules, Lot# R7-D5K1011H

April 17, 2018

Sexual Enhancement Supplement Recalled

On April 16, 2018, Epic Products, LLC, recalled its sexual enhancement supplement Euphoric because it was found to contain undeclared sildenafil and tadalafil.

April 14, 2018

Men's Sexual Enhancement Supplement Recalled

On April 12, 2018, AMA Wholesale Inc. recalled its sexual enhancement supplement Rhino 69 Extreme 50000 because it was found to contain undeclared tadalafil.

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. 

August 03, 2017

AMPT "Sexual Enhancement" Coffee Recalled

On August 1, 2017, AMPT Life, LLC, recalled all lots of AMPT Coffee after FDA testing found sildenafil and tadalafil. 

July 18, 2017

Herbal "Sexual Enhancement Coffee" Recalled

On July 13, 2017, Bestherbs Coffee LLC recalled their product New Kopi Jantan Tradisional Natural Herbs Coffee after FDA testing found desmethyl cabodenafil.

July 26, 2017

Weight Loss Supplements Containing Undeclared Drug Recalled

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

July 22, 2017

Sexual Enhancement Supplement Containing Prescription Drugs Recalled

On July 21, 2017, Ultra Shop Supplement recalled Super Panther 7K capsules after FDA testing found them to contain undeclared sildenafil and tadalafil. 

May 17, 2016

Sexual Enhancement Supplement Contains Undeclared Drugs

On May 6, 2016, the FDA issued a warning letter to Economax, LLC because the company's sexual enhancement supplement, Super Power Khan was found to contain sildenafil and hydroxyhomosildenafil.

July 18, 2017

Hidden Drugs Found in Sexual Enhancement Products

On July 17, 2017, the FDA posted public notifications after finding multiple sexual enhancement products contained hidden drug ingredients.

June 25, 2014

More Generic Versions of Heart Medication Recalled

As reported in the New York Times on June 24, 2014, certain lots of the blood pressure medication metoprolol succinate extended-release have recently been recalled. The recalling manufacturers are the Indian companies Dr. Reddy's Laboratories and Wockhardt.

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.

February 01, 2012

FDA Warns Seller of Almased Weight Loss Product of Marketing Violations

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

August 31, 2012

Energy, Fat Loss Supplement Recalled For Ephedrine Alkaloids

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

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.

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).

September 02, 2014

Recall of Weight Loss Supplement Expanded

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

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.

August 08, 2014

Weight Loss Supplement Found to Contain DMAA Recalled

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

June 23, 2013

Weight Loss Supplements Containing DMAA Recalled

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

July 24, 2013

USPLabs Destroys $8 Million Worth of Supplements Containing DMAA

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

November 20, 2013

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

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

January 31, 2014

Weight Loss Supplement Containing DMAA Recalled

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

September 27, 2013

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

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

September 15, 2013

Creatine Powder Containing DMAA Recalled

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

November 25, 2016

DMAA Product Recalled

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

February 09, 2017

Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products

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

July 20, 2017

Jail Time for Seller of Spiked Supplements

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

June 06, 2017

Seller of Vision, Cholesterol, Prostate Supplements and More Warned for Drug Claims

On May 25, 2017, the FDA issued a warning letter to Herbal Doctor Remedies following a facility inspection and review of the company's websites, www.herb-doc.com, www.ChinaSecretMed.com and www.theraherb.

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 ...

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 ...

October 27, 2004

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

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

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 ...

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, ...

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.

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, 2014

Judge Orders BioAnue To Stop Illegal Cancer and Disease Claims

On July 23, 2014, Gloria D.

April 29, 2012

FDA Says DMAA Can't Be Sold as a Supplement -- Warns Sellers

On April 27, 2012, the U.S.

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.

August 08, 2013

Weight Loss Supplement Containing Undeclared Drug Recalled

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

August 06, 2013

Weight Loss Supplement Recall Expanded

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

June 19, 2013

Weight Loss Supplements Found To Contain Undeclared Drugs, FDA Warns

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

June 19, 2013

Sexual Enhancement Supplement Found To Contain Undeclared Drug

On June 17, 2013, the FDA advised consumers not to purchase or use sexual enhancement supplement Royal Dragon Herbal Tonic Balls because it was found to contain undeclared vardenafil.

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 13, 2013

FDA Warns Consumers of Sexual Enhancement Supplements Containing Prescription Drugs

On June 10, 2013, the FDA warned consumers that a number of sexual enhancement supplements have been found to contain undeclared drugs such as sildenafil and tadalafil.

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.

March 21, 2013

FDA Warns Consumers: Three Sexual Enhancement Supplements Found To Contain Drugs

On March 21, 2013, the FDA warned consumers not to purchase or use three sexual enhancement dietary supplements, Rock-It Man, Libido Sexual Enhancer, and Stiff Days, because they were found to contain sildenafil or sildenafil analogues.

March 13, 2013

Recall: Male Sexual Enhancement Supplement Containing Drugs

On March 12, 2013, Green Planet, Inc. issued a recall of one lot of the male sexual performance enhancer supplement Night Bullet because it was found to contain trace amounts of sulfohydroxyhomosildenafil and aminotadalafil, analogues of the prescription drug sildenafil.

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.

May 08, 2013

Three Sexual Enhancement Supplements Recalled for Undeclared Drug Risk

On May 7, 2013, BeaMonstar Products issued a voluntary recall of sexual enhancement supplements SexVoltz and Velextra because they were found to contain an undeclared drug.

May 03, 2013

Recall: Two Sexual Enhancement Supplements Containing Undeclared Drugs

On May 1, 2013, American Lifestyle issued a voluntary recall of all lots of sexual enhancement supplements Vicerex and Black Ant because they were found to contain undeclared prescription drugs.

April 25, 2013

FDA Warns Consumers of Sexual Enhancement Supplements Containing Drugs

On April 25, 2012, the FDA issued a warning to consumers, urging them not to purchase or use two sexual enhancement products which were found to contain undeclared drugs.

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).

April 10, 2013

Recall: Sexual Enhancement Supplement Containing Undeclared Drug

On April 1, 2013, Consumer Concepts, Inc. issued a voluntary nationwide recall of ROCK-It MAN Male Enhancement Capsules, a dietary supplement promoted for sexual enhancement which was found to contain undeclared hydroxythiohomosildenafil, an analogue of the prescription drug sildenafil.

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.

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.

July 22, 2013

Sexual Enhancement Supplements Containing Undeclared Drugs Recalled

On July 18, 2013, Volcano Company issued a voluntary recall all lots of Volcano Male Enhancement Liquid and Volcano Male Enhancement Capsules because they were found to contain undeclared desmethyl carbodenafil, dimethylsildenafil, and dapoxetine.

July 15, 2013

Two Sexual Enhancement Supplements Recalled

On July 5, 2013, Hardmenstore.com issued a voluntary recall of 430 lots of sexual enhancement supplements Silver Sword and Clalis because they were found to contain undeclared sildenafil.

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 28, 2013

Three Sexual Enhancement Supplements Found Contain Undeclared Drugs

On June 27, 2013, the FDA warned consumers not to buy or use MVP Mega, Exten 1300 and MaxTreme Zen, dietary supplements for sexual enhancement which were found to contain undeclared tadalafil or a combination of tadalafil and sildenafil.

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 27, 2013

Another Sexual Enhancement Supplement Found Contain Undeclared Drug

On June 27, 2013, the FDA warned consumers not to buy or use Silver sword, a dietary supplement for sexual enhancement which was found to contain undeclared sildenafil.

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, ...

September 03, 2013

Sexual Enhancement Supplements Containing Undeclared Drug Recalled

On August 27, 2013, Hardmenstore.com issued a voluntary recall of sexual enhancement supplements 72HP, Evil Root and Pro Power Max because they were found to contain undeclared sildenafil.

August 23, 2013

Sexual Enhancement Supplement Containing Undeclared Drugs Recalled

On August 12, 2013, Jack Rabbit Inc. issued a voluntary recall of one lot of sexual enhancement supplement Jack Rabbit because it was found to contain undeclared sildenafil and tadalafil.

September 27, 2013

Sexual Enhancement Supplement Containing Undeclared Drug Recalled

On September 24, 2013, the FDA warned consumers not to buy or use sexual enhancement supplement Wood-E because it was found to contain sildenafil. Sildenafil, the active ingredient in the prescription drug Viagra, is typically prescribed for erectile dysfunction.

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.

November 20, 2013

Two Sexual Enhancement Supplements Found To Contain Undeclared Drugs

On November 19, 2013, Tendex issued a voluntary recall of one lot each of sexual enhancement supplements P-Boost and NatuRECT because they were found to contain tadalafil.

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 08, 2013

Sexual Enhancement Supplement Found To Contain Prescription Drugs

On November 8, 2013, the FDA warned consumers not to purchase or use sexual enhancement supplement Vitalikor Fast Acting because it was found to contain sildenafil and vardenafil.

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.

October 30, 2013

Three Sexual Enhancement Supplements Found to Contain Prescription Drugs

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

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.

October 01, 2013

Three Sexual Enhancement Supplements Containing Undeclared Drug Recalled

On September 24, 2013, Haute Health, LLC issued a voluntary recall of all lots of sexual enhancement supplements Virilis Pro, PHUK and Prolifta, because they were found to contain sildenafil.

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 31, 2014

Seven Sexual Enhancement Supplements Recalled Due to Undeclared Drugs

On March 27, 2014, Nova Products, Inc. issued a voluntary recall of sexual enhancement supplements African Black Ant, Black Ant, XZen Gold, ZXen Platinum, XZen 1200, XZone Gold and XZone 1200.

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.

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.

March 14, 2014

Arthritis and Muscle Pain Supplement Recalled

On March 12, 2014, Pain Free By Nature issued a recall of Reumofan Plus tablets sold on the company's website, www.painfreebynature.com, because it was found to contain the active pharmaceutical ingredients methocarbamol and diclofenac.

March 07, 2014

Sexual Enhancement Supplement Found to Contain Undeclared Drug

On March 7, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement Weekend Warrior because it was found to contain undeclared thiosildenafil.

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 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.

January 14, 2014

Seven Sexual Enhancement Supplements Containing Undeclared Drugs Recalled

On January 9, 2014, Midwest Wholesale issued a voluntary recall of seven sexual enhancement supplements: Boost Ultra, XZone Gold, Sexy Monkey, Triple MiracleZen Platinum, Magic for Men, "New" Extenze, and New XZen Platinum.

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.

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.

December 20, 2013

Two Sexual Enhancement Supplements Found to Contain Undeclared Drugs

On December 19, 2013, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared sildenafil or drugs chemically similar to sildenafil:

December 19, 2013

Seller of Sexual Enhancement Supplement and Tea Drink Warned for Drug Ingredients and Drug Claims

On December 5, 2013, the FDA issued a warning letter to Green Planet, Inc. following a facility inspection which found the company's sexual enhancement supplement Night Bullet to contain the drugs sulfohydroxyhomosildenafil, thioaildenafil and aminotadalafil.

November 21, 2013

Sexual Enhancement Supplement Found To Contain Multiple Drugs

On November 21, 2013, the FDA warned consumers not to buy or use sexual enhancement supplement Alpha Male because it was found to contain multiple undeclared drugs, including aminotadalafil, sulfosildenafil, sulfoaildenafil, hydroxythiohomosildenafil, dimethylsildenafil, and sildenafil.

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

Three Sexual Enhancement Supplements Recalled

On November 16, 2013, Jobbers Wholesale issued a voluntary recall of sexual enhancement supplements Rhino 5 Plus, Maxtremezen, and Extenzone because they were found to contain the undeclared drugs desmethylcarbondenafil and dapoxetine.

November 20, 2013

Another Sexual Enhancement Supplement Recalled Due To Undeclared Drugs

On November 18, 2013, Fossil Fuel Products, LLC issued a voluntary recall of sexual enhancement supplement RezzRX because it was found to contain the undeclared drugs hydroxylthiohomosildenafil and aminotadalafil.

May 29, 2014

Recall of Sexual Enhancement Supplements Expanded

On May 28, 2014, Eugene Oregon, Inc. expanded its previous recall of certain lots of sexual enhancement supplements African Black Ant, Black Ant, and Mojo Risen. All lots of these supplements are now recalled.

May 16, 2014

Sexual Enhancement Supplement Contains Hidden Drug

On May 16, 2014, the FDA warned consumers not to buy or use sexual enhancement supplement MV5 Days because it was found to contain sildenafil.

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.

July 23, 2014

Sexual Enhancement Supplement Found to Contain Hidden Drug

On July 22, 2014, the FDA warned consumers not to buy or use sexual enhancement supplement O.M.G. because it was found to contain sildenafil.

May 07, 2014

Three Sexual Enhancement Supplements Recalled

On May 5, 2014 , Eugene Oregon, Inc. issued a precautionary, voluntary recall of sexual enhancement supplements African Black Ant, Black Ant and Mojo Risen.

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.

April 18, 2014

Sexual Enhancement Supplement Contains Undeclared Drug

On April 16, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement S.W.A.G because it was found to contain sildenafil.

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.

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.

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.

August 20, 2014

Sexual Enhancement Supplement Contains Hidden Drug

On August 11, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement Arize because it was found to contain sulfoaildenafil. Sulfoaildenafil is structurally similar to sildenafil, the active ingredient in Viagra, which is prescribed for erectile dysfunction.

August 16, 2014

FDA Warns Consumers Not To Use Herbal Sexual Enhancement Supplement

On August 11, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement Herbal Vigor Quick Fix because it was found to contain tadalafil. Tadalafil is the active ingredient in the prescription drug Cialis, which is prescribed for erectile dysfunction.

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 Sexual Enhancement Supplements Found to Contain Drug

On June 17, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplements listed below because they were found to contain sildenafil.

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 06, 2014

Sexual Enhancement Supplement Found to Contain Drug

On June 5, 2014, the FDA warned consumers not to buy or use sexual enhancement supplement Zhen Gong Fu because it was found to contain sildenafil.

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.

February 10, 2015

Five Weight Loss Supplements Recalled

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

January 31, 2015

Protein Powder Recalled Due to Food Poisoning Risk

On January 30, 2015, Aloha, Inc. issued a voluntary recall of all packages of Premium Protein powder blends in chocolate and vanilla because they have the potential to be contaminated with Staphylococcus enterotoxin .

January 24, 2015

FDA Warns Consumers Not To Use Sexual Enhancement Supplement

On January 21, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Happy Passengers, because it was found to contain undeclared sildenafil. Sildenafil, the active ingredient in Viagra, which is prescribed for erectile dysfunction.

January 06, 2015

FDA Warns of Weight Loss Supplement Dangers

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

January 04, 2015

Sexual Enhancement Supplement Recalled

On December 30, 2014, Vivo Brand Management (Canada) issued a recall of one lot of the sexual enhancement supplement Forta for Men, because it was found to contain undeclared homosildenafil.

December 26, 2014

Three Sexual Enhancement Supplements Found to Contain Hidden Drugs

On December 23, 2014, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain an undeclared drug.

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.

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.

April 08, 2015

Does Your Weight Loss or Sports Supplement Contain Synthetic Amphetamine?

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

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.

May 02, 2015

Three Sexual Enhancement Supplements Contain Prescription Drug

On April 30, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplements listed below because they were found to contain sildenafil. Each was identified during an examination of international mail shipments:

April 22, 2015

FDA Warns Consumers Not to Use Male Enhancement Supplement

On April 21, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Extreme Diamond 3000 because it was found to contain desmethyl carbodenafil and dapoxetine.

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. 

August 15, 2015

FDA Warns Seller of Tainted Enhancement Supplements

On July 31, 2015, the FDA issued a warning letter to R Thomas Marketing following a review of the company's website, which found it sold the male enhancement supplements Black Ant, Herb Viagra, Real Skill and Stree Overlord . These supplements contain the undeclared sildenafil.

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.

July 01, 2015

Undeclared Drugs Found In Male Enhancement Supplements

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

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 11, 2015

Three Male Enhancement Supplements Found to Contain Drug

On March 3, 2015, the FDA warned consumers not to buy or use the following three sexual enhancement supplements because they were found to contain an undeclared sildenafil (each was identified during an examination of international mail shipments):

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 06, 2015

Four Male Enhancement Supplements Found to Contain Drug

On March 5, 2015, the FDA warned consumers not to buy or use the following four sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.

March 06, 2015

Nine Male Enhancement Supplements Found to Contain Drugs

On March 2 and March 3, 2015, the FDA warned consumers not to buy or use the following nine male sexual enhancement supplements because they were found to contain an undeclared sildenafil or vardenafil. Each was identified during an examination of international mail shipments.

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.

March 02, 2015

Four More Sexual Enhancement Supplements Found To Contain Hidden Drug

On March 2, 2015, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.

March 02, 2015

Hidden Drug Found in Six Sexual Enhancement Supplements

On February 27 and February 28, 2015, the FDA warned consumers not to buy or use the following six sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.

February 28, 2015

Drugs Found in Male Enhancement Supplements

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

May 26, 2017

"Allergy" Supplement Containing Ephedra Recalled

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

May 26, 2017

Herbal "Sexual Enhancement Coffee" Recalled, One Death Reported

On May 25, 2017, Caverflo.com issued a recall of Caverflo Natural Herbal Coffee, an "herbal" instant coffee promoted for sexual enhancement, because it was found to contain the drugs sildenafil and tadalafil. 

April 19, 2017

Sexual Enhancement Supplements for Men and Women Recalled

On April 18, 2017, Organic Herbal Supply, Inc. issued a recall of all lots of the following sexual enhancement supplements for men because they were found to contain the undeclared drug tadalafil:

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.

March 21, 2017

Twenty-one Sexual Enhancement Products Recalled

On March 7, 2017, A&H Focal Inc. issued a recall of the following sexual enhancement supplements because they were found to contain drugs such as sildenafil, tadalafil, vardenafil:

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 04, 2017

Sexual Enhancement Supplements Found to Contain Drugs

On March 3, 2017, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared drugs:

February 21, 2017

Sexual Enhancement Supplement Recalled

On February 16, 2017, Organic Herbal Supply, Inc. issued a recall of its sexual enhancement supplement XtraHRD Natural Male Enhancement because it was found to contain tadalafil.

February 09, 2017

Herbal Supplement Found to Contain Ephedra Alkaloids Recalled

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

December 19, 2017

Blue Pearl All Natural Enhancement Supplement Recalled

On December 13, 2017, Marmex Corp. recalled all lots of its sexual enhancement supplements Blue Pearl All Natural Male Enhancement Supplement, 500mg because they were found to contain undeclared sildenafil.

December 01, 2017

Nutra Labs Recalls Sexual Enhancement Supplements Containing Undeclared Drugs

On November 30, 2017, Nutra Labs Inc. recalled certain lots of its sexual enhancement supplements Bull 1800 mg Capsules and Chao Jimengnan 150 mg Tablets because they were found to contain undeclared sildenafil.

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.

May 19, 2018

Sexual Enhancement Supplements Containing Undeclared Drugs Recalled

On May 17, 2018, Shoreside Enterprises, Inc., recalled certain lots of its sexual enhancement supplements 7K and Poseidon 4500 (Extreme 1000 mg) because they were found to contain undeclared sildenafil and/or tadalafil.

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 15, 2016

Sexual Enhancement Supplements Recalled

On May 10, 2016, SOS Telecom, Inc. issued a recall of the following sexual enhancement supplements, which were found to contain undeclared sildenafil:

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.

April 16, 2016

Workout Supplement Containing Acacia Rigidula Recalled

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

April 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.

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 09, 2016

Nature Made Multis and B Complex Recalled Due to Salmonella, Staph Risk

On June 8, 2016 Pharmavite LLC issued a recall of the following Nature Made® multivitamin and B complex supplements because they have the potential to be contaminated with Salmonella or Staphylococcus aureus:

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.

February 04, 2017

FDA Warns Four Sexual Enhancement Supplements Contain Prescription Drug

The FDA recently warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared sildenafil.

February 04, 2017

Five Weight Loss Supplements Found to Contain Drugs

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

January 24, 2017

Weight Loss Supplements Found to Contain Drugs

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

December 29, 2016

Sexual Enhancement Supplement Contains Prescription Drug

On December 22, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Power Male Sexual Stimulant because it was found to contain sildenafil. This supplement was identified during an examination of international mail shipments.

December 23, 2016

Twelve Sexual Enhancement Supplements Found to Contain Prescription Drug

On December 22, 2016, the FDA warned consumers not to buy or use the following twelve sexual enhancement supplements because they were found to contain undeclared sildenafil. Each was identified during an examination of international mail shipments. 

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.

June 22, 2017

FDA Finds Hidden Drug Ingredients in Sexual Enhancement Supplements

On June 22, 2017, the FDA warned consumers that the following sexual enhancement supplements were found to contain undeclared sildenafil, tadalafil and/or dapoxetine. Use the links below to read the complete warning letter for each:

• Triple Premium Zen Gold 1300 mg

December 03, 2016

Male Enhancement Supplement Recalled

On November 29, 2016, MS Bionic, Inc. issued a recall of all lots of Megajex Natural Male Sex Enhancer capsules because they were found to contain tadalafil and sildenafil.

November 11, 2016

Male Enhancement Supplement Contains Hidden Drug

On November 9, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Ready Man! because it was found to contain sildenafil and phenolphthalein.

November 11, 2016

FDA Warns Consumers Not to Use Weight Loss Supplement

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

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:

March 20, 2016

Salute Capsules Contain Hidden Drugs

On March 17, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Salute Capsules because it was found to contain sildenafil, thiosildenafil, and sulfoaildenafil.

March 15, 2016

FDA Warns Sellers of Weight and Workout Supplements Containing Acacia Rigidula

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

April 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 04, 2016

FDA Warns Consumers Not To Use Sexual Enhancement Supplement

On March 3, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Sextra because it was found to contain sildenafil. 

February 27, 2016

Enhancement Supplement Contains Undeclared Drug

The FDA recently warned consumers not to buy or use the sexual enhancement supplement Neophase Natural Sex Enhancer because it was found to contain hydroxyacetildenafil. 

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, ...

January 22, 2016

Male Enhancement Gum and Pills Contain Hidden Drug

On January 21, 2016, the FDA warned consumers not to buy or use the following sexual enhancement supplements, because they were found to contain undeclared vardenafil (click on the name of each supplement to read the FDA's complete warning): 

January 12, 2016

Twenty-four Male Enhancement Supplements Recalled

On January 9, 2016, R Thomas Marketing LLC. in conjuction with Just Enhance LLC, issued a recall of the following sexual enhancement supplements because they were found to contain sildenafil:

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

"Tiger X" and "X Again Platinum" Contain Hidden Drugs

On December 17 and 18, 2015, the FDA warned consumers not to buy or use the following sexual enhancement supplements, which were found to contain undeclared drugs:

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.

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.

December 01, 2015

Enhancement Supplements Found to Contain Prescription Drug

On November 19, 2015, the FDA warned consumers not to buy or use the following sexual enhancement supplements, which were identified during an examination of international mail shipments, because they were found to contain undeclared sildenafil (click on the name of each supplement to read the ...

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.

November 07, 2015

Power Khan Herbal Enhancement Supplement Found to Contain Drug

On November 5, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Power Khan because it was found to contain sildenafil.

November 28, 2015

FDA Warns Consumers Not to Buy or Use "Sex Drive Capsules"

On November 19, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Sex Drive Capsules because they were found to contain sildenafil.

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.

October 24, 2015

Drug Found in Male Enhancement Supplement

On October 23, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement S.W.A.G.G.E.R Extreme because it was found to contain sildenafil.

October 17, 2015

"Herbal Viagra" Taken by Lamar Odom Was a Known Problem

It was reported this week that former NBA star, Lamar Odom, entered a coma after taking as many as 10 pills of the "herbal Viagra" formula Reload, along with cocaine.

October 14, 2015

Recall of Male Enhancement Supplement Expanded

On October 9, 2015, TF Supplements expanded its previous recall of two lots of RHINO 7 sexual enhancement supplements, which were found to contain the undeclared drugs desmethyl carbondenafil and dapoxetine, to include all lots.

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 26, 2015

Male Enhancement Supplement Containing Antidepressant Recalled

On September 25, 2015, TF Supplements issued a recall of two lots of the sexual enhancement supplement RHINO 7, which were found to contain the undeclared drugs desmethyl carbondenafil and dapoxetine.

September 16, 2015

Weight And Enhancement Supplement Recall Expanded

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

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.

July 26, 2012

Sexual Enhancement Supplements Containing Prescription Drug Recalled

On July 20, 2012, CRM Laboratories issued a voluntary recall of all X-Rock 3 Day Pill For Men and Z-Rock All Natural Male Supplements after FDA testing found these products contain the drugs sildenafil and hydroxythiohomosildenafil.

August 09, 2012

Makers of Mineral Water Containing Lithium Warned

On July 20, 2012, the FDA issued a warning letter to Lithia Mineral Water, Inc. declaring Lithia mineral water product to be an approved drug following a 2011 facility inspection.

September 21, 2012

Sexual Enhancement Supplements For Men and Women Recalled Due to Prescription Drug Risk

On August 23, 2012, Evol Nutrition Associates Inc./Red Dawn issued a voluntary recall of Mojo Nights after FDA testing revealed the male sexual enhancement supplement contains undeclared prescription drugs tadalafil and sildenafil.

September 18, 2012

Men’s Sexual Enhancement Supplement Containing Prescription Drug Recalled

On September 12, 2012, Body Basics Inc. issued a voluntary nationwide recall of ACTRA-Sx 500 Dietary Supplement Capsules after independent laboratory testing confirmed the supplement contains the prescription drug sildenafil citrate.

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 19, 2012

Sexual Enhancement Supplements Recalled Due To Undeclared Drugs

On December 17, 2012, Performance Plus Marketing, Inc.

November 09, 2012

FDA Warns Consumers of Two Weight Loss Supplements Containing a Drug

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

January 28, 2013

Recall: Male Sexual Enhancement Supplement Found to Contain Prescription Drug

On January 24, 2013, D&S Herbals, LLC, dba Freedom Trading, announced a voluntary recall of one lot of the male sexual enhancement dietary supplement Super Power because it was found to contain undeclared sildenafil.

January 24, 2013

Excessive Lead and Mercury Found In Chinese Herbal Supplements

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

January 24, 2013

"Thermo Stimulating" Supplement Recalled -- Contained DMAA

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

January 23, 2013

USPLabs Settles Class Action Lawsuit Over Controversial DMAA Ingredient

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

January 18, 2013

Recall: Iron Supplement Containing Motion Sickness Drug

On January 18, 2012, Advance Pharmaceutical Inc. announced the recall of one lot of Rugby NATURAL IRON SUPPLEMENT Ferrous Sulfate Tablets 325 mg, because the bottles were found to contain meclizine HCl 25 mg tablets instead.

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.

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.

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.

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 21, 2010

FDA Warns Consumers Not to Use Vigor-25

On November 19, 2010, the U.S.

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 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.

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.

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.

April 09, 2003

Recall of Dangerous Sexual Enhancement Supplement Illegally Containing Viagra Ingredient

On April 4, 2003, the U.S. Food and Drug Administration's MedWatch program announced that Ultra Health Laboratories, Inc. and Bionate International, Inc. are warning consumers not to purchase or consume a product known as Vinarol tablets.

May 29, 2003

Recall and Warning for Another Sexual Enhancement Supplement Illegally Containing Viagra Ingredient

On May 23, Best Life International, in cooperation with the U.S. Food and Drug Administration, warned consumers not to purchase or consume the product known as Viga.

August 08, 2017

Study Shows Severe Risk in Drinking Hydrogen Peroxide

An analysis of records from the National Poison Data System from a 10-year period ending in 2011 identified 294 reported incidents of people developing adverse symptoms after ingesting 35% (high-concentration) hydrogen peroxide (H₂0₂). Among these, 41 (13.

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.

July 01, 2005

FDA Issues Nationwide Alert for "Liqiang 4" Due to Potential Health Risk

On July 1, 2005, the U.S. Food and Drug Administration (FDA) warned consumers not to take Liqiang 4 Dietary Supplement Capsules because they contain glyburide – a drug that could have serious, life-threatening consequences in some people.

February 10, 2018

Warning to D-Limonene, Vitamin C Seller

On January 31, 2018 the FDA issued a warning letter to Long Life Unlimited, LLC following a review of the company's website which found promotional statements and testimonials made about products including Balance 600, D-Limonene, Rapha Remedy, Rapha Remedy w/ p73 Wild Oregano, Vitamin C, ...

April 01, 2004

Aloe Producer Recalls Product Due to Toxic Levels of Vitamin D

On March 26.2004, the Food and Drug Administration (FDA) announced that Aloe Commodities International, Inc., Carrollton, Texas, is recalling 1600 bottles of Solutions IE Ageless Formula II, Lot numbers P2207 and P2221 because they contain a significantly higher-than-labeled level of vitamin D3.

September 27, 2010

FTC Charges Deceptive Advertising by POM Wonderful

On September 27, 2010, the U.S.

January 03, 2004

FDA to Prohibit Sales of Dietary Supplements Containing Ephedra

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

May 28, 2003

Warning and Recall for "Herbal" Sexual Enhancement Supplement in Canada Illegally Containing Pharmaceutical Compound

On May 27, 2003 - Health Canada warned consumers not to use Hua Fo VIGOR-MAX tablets, a Chinese herbal product that contains tadalafil.

March 03, 2006

FDA Requests Seizure of More Supplements Containing Ephedrine Alkaloids

On February 24, 2006, the U.S. Food and Drug Administration (FDA) announced that the U.S.

October 18, 2005

FTC Stops False Claims about HGH Oral Spray

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

July 27, 2012

Prescription and Street Drug Alternatives Found in Male Enhancement, Mood, and Sleep Supplements

On July 10, 2012, the FDA issued a warning letter to Evol Nutrition Associates, Inc. subsequent to a 2011 inspection which found a number of the company's products contained prescription and investigational drugs and were misbranded.

August 30, 2015

Weight and Enhancement Supplements Recalled

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

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:

January 02, 2016

Fourteen Enhancement Supplements Found to Contain Undeclared Drugs

On December 28, 2015, the FDA warned consumers not to buy or use the following fourteen sexual enhancement supplements, which are sold on various websites and in some retail stores, because they were found to contain undeclared drugs :

February 13, 2016

FDA Warns Nine Sexual Enhancement Supplements Contain Undeclared Drugs

The FDA recently warned consumers not to buy or use the following sexual enhancement supplements, which are sold on various websites and in some retail stores, because they were found to contain undeclared drugs: 

November 01, 2016

FDA Warns Consumers Not to Use Twelve Energy and Sexual Enhancement Supplements

The FDA recently warned consumers not to buy or use the following "energy" and sexual enhancement supplements, which are sold on various websites and in some retail stores, because they were found to contain undeclared drugs: 

November 01, 2016

Eleven Weight Loss Supplements Contain Undeclared Drugs, FDA Warns

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

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 ...

June 04, 2014

Six Sexual Enhancement Supplements Found to Contain Hidden Drugs

On June 2, 2014, the FDA warned consumers not to buy or use the six sexual enhancement supplements listed below because they were found to contain undeclared sildenafil and tadalafil, or other drugs which are chemically similar.

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:

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.

January 30, 2014

Five Sexual Enhancement Supplements Found to Contain Prescription Drugs

On January 28, 2014, the FDA warned consumers not to buy or use the five sexual enhancement supplements listed below because they were found to contain sildenafil and/or tadalafil.

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.

May 03, 2010

FDA Warns Consumers to Avoid Breath Supplement Contaminated with Lead

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

November 04, 2016

Energy Drink Linked to Case of Acute Hepatitis

A case of acute hepatitis has been linked to daily consumption of energy drinks, according to a report published on November 1, 2016, in BMJ Case Reports.

May 15, 2018

Seller of Apple Cider Vinegar, Joint Supplements & More Warned for Drug Claims

On April 25, 2018, the FDA issued a warning letter to Baker's Best Health Products, Inc.

October 04, 2017

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

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

September 26, 2017

FDA Warns Seller of DHEA, Creatine, Chromium & More for Manufacturing Violations, Drug Claims

On August 25, 2017, the FDA issued a warning letter to Mega-Pro Nutrition, Inc., following inspections of the facility and website www.mega-pro.

June 09, 2005

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

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

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.

August 31, 2007

FTC Stops Spammers Selling Bogus Hoodia and Human Growth Hormone

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

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.).