Showing Results for Joint Max

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.

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 ...

March 12, 2026

Joint Juice $90 Million Class Action Settlement

Premier Nutrition Corporation has agreed to pay $90 million to settle a class action lawsuit alleging that its Joint Juice glucosamine products were falsely marketed to help improve joint health despite a lack of reliable scientific evidence.

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 ...

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.

April 06, 2026

Jamieson Joint Pain, Magnesium, and Maca Supplements Recalled

On April 1, 2026, Health Canada (the Canadian equivalent of the FDA) announced that Jamieson Laboratories recalled certain Jamieson Joint Pain Relief, Magnesium Bisglycinate, and Maca supplements due to defective tamper-evident seals.

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.

May 06, 2025

Joint Supplement Recalled Due to Salmonella Risk

On April 15, 2025, Optimal Carnivore, LLC recalled 1,483 bottles of Bone & Joint Restore capsules because they have the potential to be contaminated with Salmonella.

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.

December 29, 2025

Rheumacare Capsules Recalled Due to Lead

On December 22, 2025, Handelnine Global Limited (d.b.a. Navafresh), recalled certain lots of Rheumacare Capsules manufactured by Virgo UAP Pharma Pvt. Ltd. because they were found to contain elevated levels of lead.

June 16, 2020

FDA Warns Four Companies for Unsafe "Homeopathic" Injectables

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

June 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 ...

April 20, 2026

FDA Warns Consumers Not to Use Certain Pain Relief Supplements

On April 7, 2026, the FDA warned consumers not to purchase or use eight supplements labeled as containing hyaluronic acid and promoted for pain relief because they contain undeclared drugs.

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.

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.

July 16, 2024

Infla-650 Herbal Dietary Supplement Recalled

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

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.

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.

September 19, 2022

Colgate Toothpastes, Fixodent, Poligrip, & Other Personal Care Products Recalled by Family Dollar

On September 15 and 16, 2022, Family Dollar issued a recall of certain toothpastes, mouthwashes and denture adhesives, as well as other personal care products, because the products were stored and shipped outside of labeled temperature requirements.

November 28, 2022

Seller of Joint Health, Collagen Protein and More Warned for Drug Claims

On November 14, 2022, the FDA issued a warning letter to The Truth Company, LLC (parent company of Kinobody, LLC and UMZU, LLC) following inspection of the company’s websites which found statements about its Betaine, Immune, Redwood, Sensolin, Thyrite, zuRelief, Kino Aminos, Kino Collagen ...

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 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.

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.

September 28, 2022

FDA Warns Muscle Sports for Joint Health, Immune & Workout Supplement, Vitamin C, Elderberry, and Other Claims

On September 23, 2022, the FDA issued a warning letter to Muscle Sports Products, LLC following inspection of the company’s websites which found statements about company products, including Join Revolution Capsules, IMMUNITY + Powder, Rhino Rampage PUMPED Capsules, Attack Pre-Workout ...

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 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.

May 18, 2023

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

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

July 21, 2022

UV Light Wands That May Cause Injury, According to the FDA

The FDA recently warned consumers of potential exposure to unsafe levels of ultraviolet-C (UV-C) radiation associated with the use of certain brands of ultraviolet (UV) wands, as found from testing conducted by the agency.

January 15, 2024

Suprex Carb & Sugar Block Recalled

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

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.

July 22, 2024

Umary Hyaluronic Acid Supplement Recalled

On July 15, 2024, SoloVital.

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.

August 08, 2022

Woman Pleads Guilty for Selling and Promoting Products to Treat COVID-19

On July 27, 2022, Diana Daffin, owner of Savvy Holistic Health pleaded guilty to selling products with claims they could treat COVID-19 and promised “Immunity for Humans.” The products were sold under the HAMPL brand name.

November 21, 2022

Healthy Sense and People’s Choice Multis Recalled

On November 17, 2022, Mason Vitamins Inc.

April 25, 2024

Drug Found in Umary Supplement

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

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.

September 14, 2016

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

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

September 14, 2021

Seller of Lion's Mane, Other Mushroom Supplements Warned by FDA

On July 20, 2021, the FDA issued a warning letter to Brilliant Enterprises LLC because it found statements made on the company's website and social media about mushroom supplements, including Lion's Mane, BoomChaga, CordaCex, and LVL:MAX to be drug claims.

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.

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).

June 22, 2021

Living Free Vitamins, Joint, Nerve and Other Supplements Recalled

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

May 12, 2018

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

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

June 23, 2017

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

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

December 08, 2020

FTC Sends Refund Checks to Consumers of Deceptive Joint Pain Supplement Synovia

On December 1, 2020, the FTC announced it is mailing 13,221 checks totaling nearly $775,000 to consumers who bought Synovia, a supplement intended to treat joint pain and arthritis.

March 04, 2022

FTC, FDA, and DOJ Take Joint Action Against Herbal Tea Companies for COVID Claims

On March 3, 2022, the FDA, FTC, and DOJ sued a New York-based marketer of herbal tea, in attempts to permanently block deceptive ads that claim Earth Tea is clinically proven to treat, cure, and prevent COVID-19.

March 16, 2023

Omega-3 Supplements for Dogs and Cats Recalled Due to Potential for Vitamin A Toxicity

On March 9, 2023, Stratford Care USA issued a recall of 62 brands of omega-3 supplements for dogs and cats due to potentially elevated levels of vitamin A.

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 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 31, 2020

Bulletproof Warned for Manufacturing Violations

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

July 10, 2020

Seller of Thrive "Anti-Viral" Supplement Barred from Making Unproven Coronavirus and Cancer Claims

On July 10, 2020, the Federal Trade Commission (FTC) barred marketer Marc Ching from making unsubstantiated claims that the supplement Thrive can treat, prevent, or reduce the risk of coronavirus (COVID-19). Thrive consists mainly of vitamin C and herbal extracts.

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.

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.

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.

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.

April 10, 2021

Companies Deceived Consumers About Fish Oil for Liver Disease, Says FTC

On April 1, 2021, the Federal Trade Commission (FTC) announced that fish oil supplement manufacturer BASF SE and its U.S.

January 12, 2021

FDA Warns Seller of Joint and Hair Loss Products

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

January 12, 2021

FDA Warns Seller of Turmeric, Ashwagandha, Glucosamine, and More

On December 18, 2020, the FDA issued a warning letter to Reddy Naturals following a review of the company's website, which found statements made about the company's products Glycostasis, Glucosamine Curcumin, Turmeric 50, Turmeric Curcumin, Cetyl Curcumin, Ashwagandha, Huruli, ...

September 24, 2020

FTC Sends Refund Checks to Consumers of Deceptive Joint Pain Supplement

On September 24, 2020, the FTC announced it is mailing 4,782 checks totaling more than $76,000 to consumers who bought Isoprex, a supplement marketed with deceptive claims that it could treat or cure joint pain, muscle pain, headaches, and arthritis.

September 08, 2020

Holistic Healthy Pet Warned for Drug Claims

On August 25, 2020, the FDA issued a warning letter to Savvy Holistic Health dba Holistic Healthy Pet following a review of the company's website, which found statements made about some of the company's products, including Doctor's Best for Your Pets, Savvy Holistic Health Pet Essences, ...

November 20, 2020

FTC Files Complaint Against Two Supplement Companies for Deceptive Marketing

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

October 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.

December 09, 2021

FDA Warns Seller of Curcumin, Lion's Mane, Quercetin & More

On November 9, 2021, the FDA issued a warning letter to Synaptent, LLC because it found statements on the company's website about its products, including Berberine HCL, Curcumin, Lion's Man, Milk Thistle, Quercetin, Boswellia Serrata Extract, and Garlic Extract to be ...

August 17, 2021

Love & Peas Protein Rich Meal Replacement Recalled

On July 30, 2021, Nature's Sunshine issued a recall of certain lots of Love & Peas Protein Rich Meal Replacement because it may contain milk.

July 09, 2009

Recall of Whey Protein Products Due to Possible Salmonella Contamination

On July 8, 2009, the U.S. FDA announced that Max Muscle Sports Nutrition issued a voluntary recall on July 3 of Max Muscle products containing whey protein concentrate due to potential Salmonella contamination.

February 19, 2014

Seller of Sexual Enhancement Supplements Warned For Manufacturing Violations

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

November 01, 2017

FDA Warns Sellers of Bodybuilding Supplements Containing Steroid-Like Substances

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

February 11, 2020

FTC Sues Two Companies Selling Bone Health and Joint Pain Supplements

On February 11, 2020, the Federal Trade Commission (FTC) announced that it sued two companies to stop them from continuing to make false claims about their bone and joint health products, Ostinol (ZyCal Bioceuticals) and StimTein (Excellent Marketing Results, Inc. (EMR)).

December 05, 2019

Joint Supplement Synovia Was Promoted With Phony Testimonials, Says FTC

A.S. Research, LLC, has agreed to settle Federal Trade Commission (FTC) charges that they deceived consumers with false claims that their dietary supplement Synovia could treat arthritis and alleviate joint pain.

August 15, 2020

FTC Warns 20 More Companies for Coronavirus Claims

On August 14, 2020, the FTC announced that it sent warning letters to 20 companies for selling products such as vitamin C, hydrochloroquine, omega 3, and melatonin with unsupported claims that they can treat coronavirus (COVID-19).

May 10, 2021

Collagen & Biotin Supplement Recalled Due to Allergen Risk

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

February 02, 2021

Seller of Aloe Products Warned for Claiming to Treat Joint Stiffness

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

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.

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.

March 27, 2014

Bee Pollen and Weight Loss Supplements Recalled

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

November 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.

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 13, 2016

Seller of Omega-3, Ginkgo, Vision Supplements & More Warned for Drug Claims

On July 22, 2016, the FDA issued a warning letter to Viva Nutraceuticals (J & E International Corporation) following a review of the company's website and promotional literature, which found statement made about its products, Eyestonia, Ginkgo Biloba 60mg, Golden Omega-3 Max, ...

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.

September 12, 2006

U.S. Marshalls Seize Supplements Promoted as Drugs

On September 6, 2005, the U.S. Food and Drug Administration (FDA) announced that, at its request, U.S. Marshals seized quantities of Ellagimax capsules, Coral Max capsules, Coral Max without Iron capsules, and Advanced Arthritis Support capsules distributed by Advantage Nutraceuticals L.L.C.

August 01, 2017

FDA Warns Seller of Acai, Garcinia & More for Drug Claims

On July 25, 2017, the FDA issued a warning letter to Absonutrix, following a review of the company's website, www.absonutrix.com, which found statements made about some of its products to be drug claims.

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 29, 2018

Seller of Male Enhancement, Prostate Supplements & More Warned for Drug Claims

On January 10, 2018, the FDA issues a warning letter to USA Labs AKA Power Source Distributors, Inc following a review of the company's website which found statements made about its products, including Maximum Male, Beta 300 (Beta Prosturol), Chromium Max 1000, DHEA, Healthy Cold-X and ...

September 03, 2019

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

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

April 17, 2020

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

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

November 26, 2019

FDA Warns Companies Selling CBD Products as Dietary Supplements

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

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 ...

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.

July 15, 2014

Vita Springs Health Warned for Manufacturing Violations and Drug Claims

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

August 05, 2016

Seller of Fertilix Warned By FDA

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

April 03, 2015

Health Canada Suspends Sales of Male Fern Products

On April 2, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced it has suspended the licenses of the natural health products containing the ingredient male fern (Dryopteris filix-max), due to concern over the safety of the ingredient when taken at higher doses.

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

December 02, 2014

Seller of Energy & Joint Supplements, Aloe, Silver and More Warned for Drug Claims

On November 24, 2014, the FDA issued a warning letter to Jansen Enterprises, LLC, dba HealthWorksUSA, following an inspection of the company's website which found statements made about Nutra Blast Natural Energy, Ionic Silver Water, Nutra Complete, and Nutra Gel to be drug claims. 

September 10, 2014

Seller of Joint Pain Supplement Warned for Drug Claims

On August 24, 2014, the FDA issued a warning letter to CreAgri, Inc., following a website review, which found statements made about the company's products, including Olivenol plus Easeflex, Olivenol plus Essence Capsules, and Olivenol plus Essence Elixer, to be drug claims.

July 16, 2019

FDA Warns Seller of Magnesium and CBD

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

June 09, 2020

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

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

April 17, 2020

Joint Pain Supplement Isoprex Settles Charges of Making False Claims

On April 16, 2020, Renaissance Health Publishing, LLC, agreed to halt their allegedly deceptive advertising claims about their Isoprex supplement that targeted older consumers nationwide after the Federal Trade Commission (FTC) filed a complaint.

April 17, 2020

Arthritis Supplement Recalled for Salmonella Risk

On April 13, 2020, Arthri-D, LLC issued a recall of one lot of Arthri-D arthritis supplement because recent testing found it has the potential to be contaminated with Salmonella.

August 06, 2014

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

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

July 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.

November 25, 2017

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

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

May 02, 2015

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

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

June 06, 2015

Joint Supplement Contains Drugs, FDA Warns

On June 5, 2015 the FDA warned consumers not to buy or use joint pain supplement Pyrola Advanced Joint Formula because it was found to contain diclofenac and chlorpheniramine. 

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.

September 25, 2018

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

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

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.

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.

November 29, 2016

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

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

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.

September 17, 2013

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

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

October 11, 2016

Seller of Glucosamine and Chondroitin Settles FTC Charges of False Advertising

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

August 31, 2016

Seller of Joint Supplement Warned for Manufacturing Violations, Drug Claims

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

August 21, 2014

Seller of Joint Supplement Warned for Manufacturing Violations and Drug Claims

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

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.

September 25, 2018

FDA Warns Seller of Digestive Enzyme Supplements

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

March 28, 2015

Settlement Restricts Label Claims for Certain Glucosamine Supplements

On March 23, 2015 a federal judge approved a settlement agreement which will require the maker of glucosamine products (Perrigo Co.

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.

January 25, 2018

Bulletproof Collagen Protein Recalled

On January 25, 2018, Bulletproof 360, Inc issued a recall of its Bulletproof Collagen Protein supplement because it contains undeclared milk.

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.

May 30, 2017

Maker of Collagen Supplement Warned for Manufacturing Violations

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

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.

April 28, 2020

Natures CBD Oil Distribution Warned for Joint Pain Claims

On April 20, 2020, the FDA issued a warning letter to Homero Corp DBA Natures CBD Oil Distribution, following an inspection of the company's website which found the company's products, including Natures Pure CBD Oil, CBD Froggies 25mg, CBD Froggies 50mg, CBD Edibles 200mg Frogs, CBD ...

May 30, 2020

FTC Sends Refund Checks for TrueAloe and AloeCran

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

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:

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:

March 21, 2014

Products Containing Kratom Recalled Following FDA Import Alert

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

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 ...

October 10, 2014

Seller of Multivitamin Warned for Drug Claims

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

September 26, 2014

FDA Warns Seller of Supplements and Chocolate Promoted to Treat Ebola

On September 23, 2014, the FDA issued a warning letter to Natural Solutions Foundation, following a review of the company's websites which found statements made about Silver Sol Nano Silver (also called The Silver Solution) and CBD Organic Dark Chocolate Bars (also called High Potency CBD Hemp Oil) ...

July 02, 2015

Maker of Arthritis Supplement Warned for Manufacturing Violations, Drug Claims

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

June 17, 2015

Maker of Joint Supplement Warned for Manufacturing Violations

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

May 24, 2016

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

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

January 16, 2014

Joint Health Supplement Contains Dangerous Drugs, FDA Warns

On January 15, 2014, the FDA warned consumers not to buy or use joint health supplement Pro ArthMax (by Human Science Foundation) because it was found to contain multiple drugs, including diclofenac, ibuprofen, naproxen, indomethacin, nefopam, and chlorzoxazone.

June 20, 2013

Glucosamine Legal Settlement Over Labeling -- Many Products Covered

On May 16, 2013, a U.S. District Court preliminarily approved a settlement of class action cases alleging that certain claims made on the labeling of specific glucosamine products are false, deceptive, and misleading. No allegations related to safety or physical injury have been made.

February 28, 2013

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

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

August 09, 2002

Recall of 7 Herbal Products from Botanic Lab in US and Abroad

The U.S. Food and Drug Administration (FDA) released the following Class II recall information in its August 7, 2002 Enforcement Report.

August 29, 2017

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

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

January 30, 2018

Limbrel for Osteoarthritis Recalled Due to Risk of Adverse Effects

On January 26, 2018, Primus Pharmaceuticals, Inc. of Scottsdale, Arizona issued a recall of all unexpired lots of Limbrel products.

January 21, 2018

Joint Supplement Recalled for Salmonella Risk

On January 21, 2018, Arthri-D, LLC announced a recall of its joint pain supplement, Arthri-D (120 count), due to possible Salmonella contamination.

December 19, 2013

Maker of Joint Health Supplements Warned for Manufacturing Violations

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

March 01, 2013

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

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

May 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.  

September 26, 2014

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

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

September 26, 2014

Seller Warned for Promoting Essential Oils to Treat Flu, MRSA, Measles and More

On September 22, 2014, the FDA issued a warning to doTERRA International, LLC.

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 ...

November 01, 2016

Eleven Weight Loss Supplements Contain Undeclared Drugs, FDA Warns

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

May 02, 2017

Seller of Amino Acid Supplements & More Warned for Manufacturing Violations

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

April 04, 2017

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

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

April 01, 2017

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

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

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.

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 ...

August 26, 2014

Seller of Immune Supplement Warned for Drug Claims

On August 12, 2014, the FDA issued a warning letter to Ad-Med Biotechnology, following a review of the company's websites and product labels, which found statements made about Immune Active Adult Formula and Immune Active Children's Formula to be drug claims. 

May 16, 2015

FTC Mails Refund Checks to Nopalea Consumers

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

December 05, 2014

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

On November 20, 2014, the FDA issued a warning letter to Long Island Pharmaceuticals, LLC, following a facility inspection which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

December 02, 2014

Glucosamine Class-Action Settlement Reversed by Appeals Court

On November 19, 2014, an appeals court rejected a settlement of a class-action lawsuit that alleged label claims on glucosamine products manufactured or sold by Rexall Sundown, Inc., NBTY, Inc. or their affiliates, were false, deceptive or misleading.

September 26, 2015

Seller of Muscle Supplements and More Warned for Manufacturing Violations

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

September 05, 2015

Maker of Multivitamin and Fish Oil Warned for Manufacturing Violations

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

February 13, 2014

FDA Warns Consumers Not To Buy or Use Arthritis Supplement

On February 13, 2014, the FDA warned consumers not to buy or use arthritis supplement Arth-Q because it was found to contain ibuprofen.

April 24, 2014

Arthritis Supplement Containing Multiple Drugs Recalled

On April 21, 2014, Nano Well-being Health Inc., issued a voluntary recall of two lots of arthritis supplement Super Arthgold, because it was found to contain the drugs chlorzoxazone, diclofenac and indomethacin.

February 20, 2013

FDA Warns USPLabs For Adulteration and Drug Claims

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

August 29, 2012

Herbal Supplement Company Warned For Medical Claims

On August 2, 2012, the FDA issued a warning to HSAC Enterprises, Inc. dba Kare-N-Herbs subsequent to a facility inspection and website review in May 2012 which found statements made about Kold Kare, Energy Kare and Tranquility Kare dietary supplements to constitute drug claims.

January 02, 2012

FDA Warns XYMOGEN of Manufacturing and Labeling Violations Regarding Multiple Products

On December 13, 2011, the U.S. FDA sent a Warning Letter to Atlantic Pro Nutrients, Inc. (dba XYMOGEN) regarding labeling and/or manufacturing violations relating to its products, which include Borage CP-240, CoQmax CF, Immune Rx, Iron Glycinate, and Green Tea 600.

October 05, 2011

FDA Warns Nature's Rite of Promoting 8 Supplements as Drugs

The FDA published a Warning Letter dated September 19, 2011 to Nature's Rite, LLC stating that the firm’s online promotion of its various supplements for the treatment or prevention of various diseases cause these products to be considered unapproved drugs.

September 23, 2014

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

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

October 13, 2018

Pharmaceutical Drugs Found In Dietary Supplements Pose Danger to Consumers

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

June 21, 2002

Canadian Warning on Use of Seven Herbal Supplements from BotanicLab

On June 19, 2002, Health Canada issued a warning that Canadians not use seven herbal products manufactured in the United States by BotanicLab because they contain undeclared prescription drugs that could cause serious health effects if not taken under medical supervision.

March 28, 2008

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

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

September 05, 2014

Seller of "Nerve", "Cleanse" and Probiotic Supplements Warned for Drug Claims

On July 30, 2014, the FDA issued a warning letter to Plexus Worldwide, Inc., following a review of the company's website and product labels, which found statements made about Fast Relief, BioCleanse and ProBio5 to be drug claims.

May 03, 2011

FDA Warns: Beware of Bogus STD Products

On May 3, 2011, the U.S. Food and Drug Administration (FDA) and the Federal Trade Commission (FTC) announced a joint effort to remove products from the market that make unproven claims to treat, cure, and prevent sexually transmitted diseases (STDs).

June 21, 2010

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

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

April 11, 2008

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

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

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 28, 2013

Maker of Liquid Omega-3 Supplements Warned For Manufacturing Violations

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

June 13, 2012

Tart Cherry Supplement Selller Warned by FDA Over Illegal Health Claims

The U.S. FDA recently published a Warning Letter (dated June 8, 2012) to Michelle's Miracle, Inc. for illegally promoting a range of tart cherry dietary supplements using health claims reserved for drugs. The products cited are: 

May 07, 2012

FDA Warns Doctor Promoting Own Supplements Online as Treatments

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

January 04, 2012

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

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

May 10, 2013

Protein Extract Recalled for Undeclared Allergens

On May 6, 2013, Pure Herbs Ltd. issued a voluntary recall of Protein Extract because it contains undeclared milk and soy allergens.

August 26, 2014

Supplement Maker Warned for Manufacturing Violations

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

October 25, 2016

Seller of Liquid Aloe & Mineral Supplement Warned for Manufacturing Violations

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