Reviews and Information for Just Ingredients

July 25, 2024

West Coast Laboratories Warned for Manufacturing, Labeling Violations

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

July 23, 2025

FDA Warns Seller of Allegro Eye Drops, Tea Tree Oil Eyelid Wipes, and More

On July 9, 2025, the FDA issued a Warning Letter to Scope Health Inc.

February 22, 2024

Pacific BioLogic Co. Warned by FDA for Manufacturing Violations

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

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.

September 24, 2024

Manufacturer of Mushroom Gummies Warned by FDA for Violations

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

October 20, 2025

FDA Warns Vidaslim for Manufacturing Violations

On July 17, 2025, the Food and Drug Administration issued a Warning Letter to Vidaslim Co.

January 24, 2020

Fat-Burning, Energy Supplement Linked to Heart Trouble

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

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.

November 06, 2023

FDA Warns Consumers Not to Use Dr. Ergin’s SugarMD Advanced Glucose Support, Found to Contain Prescription Drugs

On November 3, 2023, the FDA warned consumers not to purchase or use Dr. Ergin’s SugarMD Advanced Glucose Support products after FDA laboratory analysis found the supplement to contain glyburide and metformin.

September 25, 2023

FDA Warns Consumers Not to Use Tapee Tea

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

January 15, 2024

5 Star Nutrition Will Pay $4.5 Million for Selling Misbranded Workout Supplements

On January 12, 2024, Defyned Brands, also known as 5 Star Nutrition LLC, pleaded guilty in federal court to three-counts of distributing misbranded dietary supplements following an investigation by the Food and Drug Administration’s Office of Criminal Investigations (FDA-OCI).

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.

September 05, 2024

Don’t Buy or Use Umary and Amazy Supplements, Warns FDA

On September 5, 2024, the FDA warned consumers not to purchase or use Umary Hyaluronic Acid or Amazy Hyaluronic Acid supplements because testing by the agency found them to contain diclofenac and omeprazole.

September 01, 2022

Elite One Source Nutritional Services Warned for Manufacturing, Labeling Violations

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

July 16, 2025

Organic and Mineral Sunscreens, Tints, Recalled

On March 12, 2025, Kabana Skin Care recalled four brands of organic and/or mineral sunscreen products due to unspecified "deviations" in Current Good Manufacturing Practices (cGMPs).

September 25, 2025

FDA Warns Consumers Not to Use Joint Pain Supplement FTX PLUS

On September 5, 2025, the FDA advised consumers not to purchase or use FTX PLUS, a product promoted for joint pain on various websites, including Walmart and possibly in some retail stores.

March 23, 2026

FDA Warns Consumers Not to Use ULTRA ADVANC3 Joint Supplements

On February 26, 2026, the FDA warned consumers not to purchase or use ULTRA ADVANC3 and ULTRA ADVANC3 GOLD, products promoted for joint pain relief, because FDA testing found that they contain undeclared dexamethasone, diclofenac, and methocarbamol, which are not permitted in ...

April 08, 2026

FDA Warns Consumers Not to Use Addall Shots or Supplements

On April 3, 2026, the FDA warned consumers not to use Addall XR Shot and Addall XL capsules, products promoted for energy and focus, after FDA testing found they contain undeclared drug ingredients that are not permitted in dietary supplements and may pose serious health risks.

June 26, 2024

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

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

December 19, 2024

Force Forever Joint Pain Supplement Recalled

On December 12, 2024, GNMart INC recalled all lots of Force Forever, a supplement promoted for joint pain, because FDA tests found it to contain undeclared diclofenac and dexamethasone.

November 18, 2024

Manufacturer of Grandma’s Herbs Kidney Warned by FDA

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

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.

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.

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.

June 13, 2022

“Natural” and OTC Mole, Skin Tag Removal Products Can Be Dangerous, Warns FDA

On June 9, 2022, the FDA warned consumers not to use “natural” or over-the-counter (OTC) products promoted to treat or remove moles, skin tags, and seborrheic keratoses because they can contain potentially dangerous concentrations of salicylic acid or other harmful ingredients.

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).

April 25, 2024

Yogi Tea Recalled Due to Pesticides

On April 19, 2024, Yogi Tea issued a recall of over 54,800 packs of Yogi Echinacea Immune Support tea after a sample of echinacea tested above acceptable limits for multiple pesticides. No illnesses have been reported to date.

November 09, 2023

Zazzee Naturals Warned for MSM Eye Drop Claims

On October 30, 2023, the FDA issued a Warning Letter to Dexterity Health, LLC DBA Zazzee Naturals following review of the company’s Amazon storefront, which found statements about the company’s Liquid MSM Drops to be drug claims.

December 14, 2023

FDA Warns Seller of Novid NASAL SPRAY for Allergy, Virus, and Cold Claims

On December 7, 2023, the FDA issued a warning to Novid Group, Inc. following an inspection of the company’s website, which found statements about the company’s novid NASAL SPRAY product to be drug claims.

December 14, 2023

Pain Relief Tea Recalled, Found to Contain Prescription Drugs

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

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.

October 05, 2023

Counterfeit Pure Encapsulations and GutConnect 365 Sold on Amazon

On September 26, 2023, a man from New Jersey was arrested for selling fake versions of Pure Encapsulations L-Glutamine and Nature MD's GutConnect 365 on Amazon.

July 17, 2023

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

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

June 19, 2018

FDA Warns Seller of Weight Control Patches

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

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.

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 28, 2015

GNC Accused of Selling Supplements with Unlawful Ingredients

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

December 13, 2013

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

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

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.

July 22, 2024

Umary Hyaluronic Acid Supplement Recalled

On July 15, 2024, SoloVital.

November 21, 2024

Umary Hyaluronic Acid Sold on Amazon Recalled

On November 20, 2024, MXBBB issued a recall of one lot of Umary Hyaluronic Acid or Amazy Hyaluronic Acid supplements, which were sold on Amazon.

January 26, 2023

FDA Warns Seller of Canary Seed Omega-3

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

May 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.

June 16, 2022

Omega 3 Supplements Recalled Due to Undeclared Drug Ingredients

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

July 20, 2023

FTC Files Complaint Against Company Promoting “Sobrenix” Supplements for Alcohol Cravings

On July 19, 2023, the FTC filed a complaint against Rejuvica and the company owners for promoting its Sobrenix supplements, which contain ingredients such as vitamin B6, thiamin, milk thistle, Chanca Piedra, and dandelion root, to reduce and eliminate alcohol cravings and consumption.

November 29, 2023

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

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

May 29, 2025

Umary Joint Pain Supplements Recalled

On May 21, 2025, UMARY USA recalled all lots of Unavy Ácido HIALURÓNICO (30 caplets/850 mg) and Umovy Ácido HIALURÓNICO (30 caplets/850 mg).

November 12, 2017

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

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

July 24, 2017

Protein Bars Recalled Due to Listeria Risk

On July 21, 2017, Bhu Foods recalled a number of their products after their organic sunflower seeds, distributed by Hudson Valley Foods, Inc., were potentially contaminated with Listeria monoocytogenes.

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.

February 17, 2012

FDA Warns Supplement Company of Manufacturing Violations

The U.S. FDA recently posted a Warning Letter to Pure Encapsulations, Inc.

April 25, 2013

Vision Supplement Company Warned For Drug Claims

On March 15, 2013, the FDA issued a warning letter to Synticare Corp. because statements made on the company's website about certain supplements, including Maximum Lutein, AREDS 1, AREDS 1 Smokers, AREDS 2, Combo AREDS 1 and 2, and Combo Smokers AREDS 1 and 2, were found to be drug claims.

May 14, 2016

Xylitol in Supplements Poses Danger for Dogs

On May 12, 2016, the FDA warned consumers that xylitol, a popular sweetener found in chewable vitamins, chewing gum, breath mints, toothpaste and a variety of other products, is toxic to dogs.

November 11, 2014

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

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

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.

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 ...

December 15, 2022

Beware of Supplements, Homeopathic Products Promoted to Treat Flu, Says FDA

On December 13, 2022, the FDA warned consumers to beware of supplements and homeopathic products, as well as nasal sprays, sanitizers and other products that promise to prevent or treat the flu.

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).

January 09, 2009

FDA Expands Warning to Consumers About Tainted Weight Loss Pills

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

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.

December 19, 2020

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

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

February 25, 2017

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

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

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.

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.

November 03, 2009

Recall of 65 Dietary Supplements That May Contain Steroids

On November 3, 2009, as part of its ongoing cooperation with the Food and Drug Administration ("FDA"), Bodybuilding.

August 31, 2004

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

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

June 16, 2020

FDA Warns Four Companies for Unsafe "Homeopathic" Injectables

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

May 11, 2022

FDA Warns 10 Companies for Selling Workout Supplements With Dangerous Ingredients

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

April 24, 2024

NOW Solutions XyliWhite Coconut Oil Toothpaste Gel Recalled

On March 6, 2024, NOW Foods issued a recall of over 27,000 units of NOW Solutions XyliWhite Coconut Oil Toothpaste Gel because it has an off taste and flavor.

November 21, 2010

FDA Warns Consumers Not to Use Vigor-25

On November 19, 2010, the U.S.

April 07, 2008

Federal Agents Seize Nearly $1.3 Million of Illegal Dietary Supplements

On April 4, 2008 the U.S. FDA announced that, at its request, U.S. Marshals had seized more than $1,301,712 of dietary supplements from LG Sciences, LLC, of Brighton, Mich.

May 13, 2009

Body-Building Supplements Confiscated by FDA for Adulteration

On May 11, 2009, the U.S. FDA announced that U.S. Marshalls seized more than 23,300 bottles of three dietary supplement products distributed by LG Sciences LLC, of Brighton, Mich.

July 19, 2012

FDA Warns Company Selling Mineral Supplements as Treatments

On June 28, 2012, the FDA issued a warning letter to Prismic Light International for multiple Good Manufacturing Practices (GMP) violations, promoting dietary supplements as drugs, and misbranding products.

September 01, 2011

Recall of Prenatal Supplement Due to Egg Allergen

According to the FDA website, on August 31, 2011, Pure Encapsulations announced the voluntarily recall of it "PreNatal Nutrients" supplement, lot number 3560111, because it may contain undeclared egg allergen.

July 15, 2011

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

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

July 03, 2012

Standard Process Recalls Three Supplements Due to Possible Salmonella Contamination

On June 29, 2012, Standard Process issued a voluntary recall of the company's Cataplex ACP, Cataplex C and Pancreatrophin PMG, after a routine FDA inspection uncovered potential Salmonella contamination in an ingredient found in these three products.

February 13, 2013

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

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

May 02, 2020

Seller of Botanical and CBD Oil Patches Warned for Coronavirus Claims

On April 27, 2020, the FDA issued a warning letter to Santiste Labs LLC for promoting its transdermal patches containing botanical oils and/or CBD with unsupported claims that they can treat coronavirus (COVID-19).

October 29, 2019

Chinese Herbal Supplement May Raise PSA

Use of a Chinese herbal supplement appears to have significantly increased the PSA (prostate specific antigen) level in a man treated for prostate cancer, erroneously suggesting a recurrence of the cancer (Abel, J Am Osteopath Assoc 2019).

October 29, 2019

Publisher Sued for Promoting "Phony Diabetes Cure"

On October 24, 2019 the FTC filed a lawsuit against the publisher of books, newsletters, and other publications aimed at seniors that falsely promise to cure type 2 diabetes.

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

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. 

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.

November 16, 2018

Two Popular Memory Supplements Missing Some or All of Key Ingredient

Two popular Ginkgo biloba supplements marketed to improve memory do not contain the Ginkgo biloba claimed on their labels, according to tests conducted by the U.S. Government Accountability Office (GAO).

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).

January 18, 2003

Non-Prescription Anti-Hypertension Pills Recalled

On January 17, the U.S. FDA's MedWatch Program reported that Herbsland Inc.

March 01, 2013

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

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

February 20, 2013

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

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

December 27, 2012

Two Supplement Companies Warned For Manufacturing Violations

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

December 06, 2013

Weight Loss Supplement Claims Challenged

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

December 19, 2013

Maker of Joint Health Supplements Warned for Manufacturing Violations

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

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.

October 29, 2016

Steroid "Alternatives" Not Permitted In Dietary Supplements, FDA Warns

On September 27, 2016, the FDA issued a warning letter to Proprietary Wellness, L.L.C.

July 23, 2016

Seller of GlucoCor Warned for Drug Claims

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

September 10, 2012

Maker of Concussion Recovery Supplement Warned For Making Drug Claims

On August 28, 2012, the FDA issued a warning letter to Trinity Sports Group, Inc. after a review of the company's websites found statements about Neuro Impact Concussion Response Formula constituted drug claims not permitted on supplements. 

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.

January 16, 2010

Recall of Body Building Supplements Containing Steroids

On January 15, 2010, the Food and Drug Administration (FDA) posted a voluntary recall notice from MuscleMaster.com, Inc. regarding all lots and expiration dates of seventeen dietary supplements sold in 2009 from June 1 and Novemember 17.

February 03, 2015

Major Retailers Accused of Selling Adulterated Herbal Supplements

On February 3, 2015, the New York State Attorney General announced that his office sent letters to four major retailers, GNC, Target, Walmart, and Walgreens, for allegedly selling store brand herbal supplement products in New York that either could not be verified to contain the labeled substance, ...

November 21, 2014

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

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

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.

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.

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.

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.

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.

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.

July 09, 2010

FDA Issues Warning on Herbal Weight Loss Supplement

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

September 25, 2012

Whey Protein Supplements Recalled Due To Undeclared Allergens

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

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.

June 27, 2012

Maker of Pain Relief, Virility, and Idebenone Products Warned of Violations by FDA

On June 19, 2012, the U.S. FDA warned ABCO Laboratories of Fairfield, Caliornia, a contract manufacturer, of violations of FDA regulations for its products IBU-RELIEF 12, Sexual Virility Max, and Idebenone Capsules.

April 18, 2014

FDA Questions Ingredient in Workout Supplement

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

January 16, 2015

CVS Sued for Eye Health Supplement Claims

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

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.

April 11, 2013

Chinese Herbal Manufacturer Warned For CGMP Violations

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

October 18, 2012

Natural Product Manufacturer Warned For GMP Violations, Misbranding, Unapproved Devices and Drug Claims

On August 28, 2012, the FDA issued a warning letter to Creation's Garden Natural Products, Inc. following an inspection of the company's manufacturing facility, which found violations of Current Good Manufacturing Practices (CGMPs) for dietary supplements.

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.

February 19, 2005

Seller of Eye Supplement Purporting to Restore Vision and Eliminate "Floaters" Settles FTC Charges

On February 15, 2005, the Federal Trade Commission (FTC) announced that Hi-Health Supermart Corporation (Hi-Health) and its owner, Simon Chalpin, have settled FTC charges that they made unsubstantiated advertising claims that their product – Premier Formula for Ocular Nutrition-Optim3 (Ocular ...

May 20, 2005

Seller of "Ocular Nutrition" Supplement Settles FTC Charges

On March 16, 2005, The Federal Trade Commission (FTC) announced that Hi-Health Supermart Corporation (Hi-Health) and its owner, Simon Chalpin, settled FTC charges that they made unsubstantiated advertising claims that their product – Premier Formula for Ocular Nutrition-Optim3 (Ocular Nutrition) – ...

June 17, 2004

FTC Challenges Deceptive Weight Loss Claims for Supplement Targeted at Hispanics

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

November 02, 2012

Manufacturer of Prostate, Inflammation and Cholesterol Supplements Warned For Drug Claims

On October 15, 2012, the FDA issued a warning letter to Ortho Molecular Products, Inc. for making drug claims about the following dietary supplements: Candicid Forte, Inflamma-bLOX, Lipitrol, Mucosagen, Prostatrol Forte, Resvoxitrol, Paracid Forte, VascuPak HTN and Lithium Orotate.

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.

June 07, 2012

Recall of Digestive Health Supplement Due to Salmonella Concern

On June 4, 2012, Botanical Laboratories of Ferndale, WA announced the recall of 38 bottles of 33.8 oz Wellese "Digestive 3 in 1 Health " liquid dietary supplement and 275 bottles of 16 oz.

June 05, 2012

Many "Grapefruit Seed Extracts" Adulterated

On June 4, 2012, the American Botanical Council (ABC) announced the publication of a review of scientific literature regarding “grapefruit seed extracts,” raising concerns about apparent adulteration of products in the US and international marketplaces.

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 29, 2009

FDA Warns Against Body Building Supplements with Steroid-like Compounds

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

May 01, 2009

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

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

March 13, 2020

FDA Finds Problems at 52% of Supplement Manufacturing Sites in U.S. and 42% Abroad

ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2019 (October 1, 2018 - September 30, 2019) of 598 dietary supplement manufacturing facilities in the U.S.

July 01, 2003

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

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

January 17, 2006

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

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

January 11, 2002

Canada Requests Recall of Certain Ephedra/Ephedrine Products

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

May 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 01, 2013

Maker of Algae Products Warned For Drug Claims, Manufacturing Violations

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

May 09, 2013

Joint Health Supplement Recalled for Undeclared Allergens

On May 1, 2013, XYMOGEN issued a voluntary recall of the joint health supplement artriphen, because it contains undeclared soy and milk allergens.

May 03, 2013

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

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

October 17, 2012

Herbal Supplement Company Warned For Manufacturing Violations and Drug Claims

On October 2, 2012, the FDA issued a warning letter to Amazing Herbs Nutraceuticals following a facility inspection which found violations of Current Good Manufacturing Practices (CGMPs) for dietary supplements.

February 13, 2013

Herbal Supplement Maker Warned For Manufacturing Violations, Misbranding

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

February 04, 2013

Protein Supplement Recalled Due To Undeclared Soy and Milk

On January 30, 2013, R-Kane Products, Inc. issued a recall of Z PRO HIGH PROTEIN SUPPLEMENT after an FDA inspection found the potential allergens soy and milk were not listed on individual packet labels of the supplement.

February 21, 2015

FTC Mails Refund Checks to Consumers Who Purchased Weight Loss Pills

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

December 12, 2014

FTC Mails Refund Checks to Consumers Who Purchased Sensa

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

December 05, 2015

FDA Warns Companies Selling Products Containing Picamilon

On November 30, 2015, the FDA issued warning letters to five supplement companies selling products containing picamilon, which is not a lawful dietary supplement ingredient in the U.S.

April 03, 2014

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

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

March 19, 2014

Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations

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

July 15, 2014

Pinnacle Labs International Warned for Manufacturing Violations

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

June 24, 2014

CELLFOOD Recalled in Canada

On June 23, 2014, Health Canada recalled CELLFOOD (Nu Science), a supplement promoted for improved energy, endurance and natural health, because it was found to be an unauthorized health product.

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.

August 02, 2012

FDA Warns Two Supplement Makers of Manufacturing Violations

On July 19, 2012, the FDA issued a warning letter to H & L Jerch Sales, Inc. for failing to maintain written quality control procedures, which constitutes a violation of current Good Manufacturing Practices (cGMP) and caused the company’s products to be declared adulterated.

April 07, 2011

FDA Warns Manufacturer of Soy Products of Violations

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

October 18, 2011

FDA Warns Consumers Against Eighteen Weight Loss Products Containing Drugs

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

July 13, 2012

FDA Warns of Aloe Drug Claims and Misbranding

On June 12, 2012, the FDA issued a warning letter to Set-N-Me-Free Aloe Vera Company concerning twelve of the company's products. Based on how the products were promoted, the FDA regards the products as unapproved new drugs and misbranded, with labels that provided inadequate directions for use.

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.

March 03, 2012

FDA Warns Vitaganic of Manufacturing Violations

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

May 16, 2005

Athlete Wins Case Involving Contaminated Vitamin

On May 13, 2005 the Associated Press reported that a swimmer, who claimed a contaminated vitamin caused him to test positive for steroids, won $578,635 in a lawsuit against a maker of dietary supplements.

December 10, 2002

Company Ordered to Cease Deceptive Marketing of Weight Loss Product

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

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.

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. 

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.

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. 

January 04, 2007

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

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