Showing Results for Herbal Select

March 01, 2023

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

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

March 09, 2022

FDA Warns Seller of Magnesium, CBD, Herbal Extracts & More

On February 9, 2022, the FDA issued a warning letter to Bea Lydecker’s Naturals, Inc.

December 20, 2021

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

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

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.

March 23, 2023

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

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

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.

September 06, 2022

Sand Ginger Powder Recalled in Canada Due to Aconite

On September 1, 2022, Ka Wing Hong issued a recall of Mr. Right brand Keampferia Galanga Powder (sand ginger powder), a common spice used in Asian cuisine, due to aconitine contamination.

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.

July 19, 2023

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

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

October 19, 2023

Jay Robb Protein Powder Recalled

On October 13, 2023, Select Custom Solutions recalled one lot of Jay Robb Vanilla Flavored Egg White Protein 24 oz because the product may contain hard, plastic, foreign material which could pose a choking hazard. No adverse events have been reported to date.

September 16, 2015

Herbal Extracts Recalled

On September 15, 2015, Iowa Select Herbs, LLC issued a recall of numerous herbal exacts following a permanent injunction which required the company to stop selling supplements.

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.

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).

December 01, 2022

FTC Takes Action Against Company Promoting “COVID Resist” Supplement to Treat COVID-19

On November 22, 2022, the FTC filed a complaint in a U.S. district court against California-based company Precision Patient Outcomes, Inc. for promoting its COVID Resist and VIRUS Resist supplements to prevent and treat COVID-19.

December 12, 2022

FDA Warns Saffron USA for Promoting Teas to Treat Insomnia, Osteoporosis & Cancer

On September 23, 2022, the FDA issued a warning letter to Saffron USA LLC following inspection of the company’s website which found statements about its Allergy Blend, Chamomile Tea Petals, Diabetic Support Blend, Orange Blast Tea, and Saffron Loose Tea products to be drug ...

December 29, 2022

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

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

August 17, 2022

Seller of Moringa Tea and Other Herbal Products Warned for Drug Claims, Manufacturing Violations

On July 29, 2022, the FDA issued a warning letter to Deggeh Foods, Inc.

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.

August 23, 2015

Maker of Herbal Supplements Sold on eBay, Amazon and Other Websites Shut Down

On August 17, 2015, a federal court ordered a permanent injunction against dietary supplement company Iowa Select Herbs LLC for unlawfully manufacturing and distributing unapproved new drugs and misbranded drugs and adulterated and misbranded dietary supplements.

December 29, 2020

FDA Warns Five Sellers of CBD for Claims of Treating Arthritis, Alzheimer's and More

On December 22, 2020, the FDA issued warning letters to five sellers of CBD following reviews of the companies' websites, which found statements made about the companies' products to be drug claims.

July 07, 2020

Sellers of Essential Oils, Hand Sanitizers and More Warned for Coronavirus Claims

The FDA recently issued warning letters to five companies for selling products such as essential oils, homeopathic products, and Chinese herbal products with unsupported claims that they can treat coronavirus (COVID-19).

July 10, 2020

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

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

December 15, 2020

FDA Warns JC Ayur Life LLC for Drug Claims

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

November 23, 2022

CBD Not Permitted in Gummies, Candies, Cookies, Candy, or Pet Treats, Says FDA

On November 16, 2022, the FDA issued warning letters to five companies for selling products such as gummies, tea, cookies, lollipops, fruit snacks, hard candies, and pet treats containing cannabidiol (CBD) and/or delta-8 tetrahydrocannabinol (delta-8 THC) as conventional food products.

October 12, 2020

Griffo Botanicals Warned for COVID-19 Claims

On October 7, 2020, the FDA issued a warning letter to Griffo Botanicals for selling various herbal products, including BaseCamp, Gan Mao, Febris, Fortifend, Xiao Chai Hu, HuBei #1, Qing Fei Pai Du, Solis, and WuHan #2, with unsupported claims that they can treat coronavirus ...

October 12, 2020

Prairie Dawn Herbs Warned for COVID-19 Claims

On October 7, 2020, the FDA issued a warning letter to Prairie Dawn Herbs for selling various herbal products with unsupported claims that they can treat coronavirus (COVID-19).

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.

November 05, 2021

Herb Recalled Due to Risk of Lead, Cadmium Contamination

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

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.

December 08, 2015

Study Finds Many Rhodiola Rosea Supplements to be Adulterated

A study of Rhodiola supplements (including hard capsule extracts, softgel capsules, tablets, and liquid extracts) in Great Britain found that nearly 20% did not contain rosavin, the key marker compound used to identify Rhodiola rosea from other Rhodiola species, and many ...

May 23, 2020

FTC Warns 50 More Companies for Coronavirus Claims

On May 21, 2020, the FTC announced that it sent warning letters to 50 companies for selling products such as herbal products, immune system boosters, and vitamin C, with unsupported claims that they can treat coronavirus (COVID-19).

May 09, 2020

FTC Warns 45 More Companies for Coronavirus Claims

On May 7, 2020, the FTC announced that it sent warning letters to 45 companies for selling products such as herbal products, immune system boosters, and vitamin C with unsupported claims that they can treat coronavirus (COVID-19).

July 27, 2019

Herbal Doctor Remedies Recalls 43 Products

On July 24, 2019, Herbal Doctor Remedies issued a recall of 43 Chinese herbal medicines, including Bone Fixer, Lipidtrol, Pain Away, Prostatin, Stomach Flu and others, because they were marketed without FDA approval and were manufactured outside of the controls required by current Good ...

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).

June 04, 2020

FTC Warns 35 More Companies for Coronavirus Claims

On June 4, 2020, the FTC announced that it sent warning letters to 35 companies for selling products such as herbal products, immune system boosters, and vitamin C with unsupported claims that they can treat coronavirus (COVID-19).

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).

June 02, 2020

Sundial Herbal Ordered to Halt Distribution of Products

On June 1, 2020, a New York federal judge filed an order against two individuals doing business as Sundial Herbal Products to stop the company from distributing its products, which were found to be misbranded and promoted as drugs.

October 01, 2019

Lead and Arsenic Found in Multi Mineral & Vitamin Supplement

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

March 09, 2020

FDA Warns Sellers of Essential Oils, Colloidal Silver & Teas Promoted to Treat Coronavirus

On March 9, 2020, the FDA and FTC announced they have issued joint warning letters to seven companies for selling products such as essential oils, teas and colloidal silver with unsupported claims that they can treat coronavirus (COVID-19).

October 19, 2020

Seller of Thrive "Anti-Viral" Supplements Settles with FTC for Unproven Coronavirus and Cancer Claims

On October 19, 2020, the Federal Trade Commission (FTC) approved an administrative consent order to settle charges that marketer Marc Ching was making unsubstantiated claims that the supplement Thrive can treat, prevent, or reduce the risk of coronavirus (COVID-19).

March 04, 2021

Federal Court Bars Confidence USA from Selling Supplements

On March 4, 2021, the FDA announced a permanent injunction has been entered, barring dietary supplement manufacturer Confidence USA Inc. and two of its executives from producing or selling products until they become compliant with current good manufacturing practices (cGMPs).

July 17, 2020

Sellers of Immune Boosters, Vitamin C Warned for Coronavirus Claims

The FDA recently issued warning letters to two companies for selling products such as immune boosters, vitamin C, and zinc with unsupported claims that they can treat COVID-19 (use the links below to read the full warning letter):

June 20, 2020

FTC Warns 30 More Companies for Coronavirus Claims

On June 18, 2020, the FTC announced that it sent warning letters to 30 companies for selling products such as immune system boosters, colloidal silver, vitamin C, and CBD with unsupported claims that they can treat coronavirus (COVID-19).

May 06, 2014

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

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

February 04, 2020

Seller of Digestion Supplements Warned for Manufacturing Violations

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

March 29, 2020

Seller of "Immune Tonic" Warned for Making Coronavirus Claims

On March 26, 2020, the FDA issued a warning letter to Carahealth for selling products with unsupported claims that they can treat coronavirus (COVID-19).

August 14, 2020

The Green Herb and New Genesis Health Warned for Manufacturing Violations

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

July 21, 2020

51 CBD Products Recalled Due to Lead Contamination

On June 23, 2020, InHe Manufacturing, LLC and MHR Brands issued a recall of fifty-one CBD products due to contamination and/or potential with lead. Thirty-six of the products are marketed for people and fifteen of the products are marketed for pets.

June 26, 2015

Seller of CoQ10, Anxiety Supplements and More Warned for Manufacturing Violations, Drug Claims

On June 6, 2015, the FDA issued a warning letter to Country Doctor Herbals, following a facility inspection which found the company's products, including  Herbal Flu Be-Gone, Herbal Multi-Bac, Herbal Nervine, Herbal Pain-A-Way, Herbal Pancreas, Herbal Parasite Cleanse, Herbal Perfect ...

August 26, 2014

Maker of Herbal Supplements Warned for Manufacturing Violations and Drug Claims

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

January 16, 2014

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

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

August 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.

July 03, 2018

Seller of Chinese "Cancer" Supplements Warned

On June 26, 2018, the FDA issued a warning letter to the American Chinese Medicine Association (ACMA), following a a review of the company's website, which found statements made about its products, including ACMA Brain Tumor Treatment, ACMA Breast Cancer Treatment, ACMA Colon Cancer ...

January 10, 2013

FDA Warns Aloe and Herbal Supplement Companies For Manufacturing Violations

AloeScience Labs, Inc. -- On November 14, 2012, the FDA issued a warning letter to AloeScience Labs, Inc.

August 25, 2009

Hepatitis Associated with Herbal Supplement Containing Artemisinin

The August 14, 2009 edition of the Center for Disease Control's (CDC) Morbidity and Mortality Weekly Report includes case report of hepatitis associated with use of an herbal supplement containing artemisinin.

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, ...

March 17, 2015

Seller of Tea Warned for Drug Claims

On March 4, 2015, the FDA issued a warning letter to Four Elements Organic Herbals, LLC because statements made about HERBAL TEA Power, Energy & Stamina, ORGANIC HERBAL TEA Tulsi TelepaTea, ORGANIC HERBAL TEA To Your Health, Hawthorn Fresh Herb Extract, Elderberry Fresh Herb ...

December 18, 2006

Canada Warns of Herbal Sleep Product Containing Rx Drug

On December 18, 2006 Health Canada advised consumers not to use a product called Eden Herbal Formulations Sleep Ease Dietary Supplement, because it was found to contain an undeclared drug estazolam, which can be habit-forming when used for as little as a few months.

June 20, 2003

Mixing Herbal Supplements, Migraine Medications Can Be Dangerous

On June 19, 2003, ABC News reported than an extensive review of existing research has led University of Utah researchers to conclude several popular herbal supplements may cause adverse, even deadly, reactions when combined with certain migraine medications.

July 03, 2018

FDA Warns Seller of Adulterated Chinese Herbal Supplements

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

November 08, 2016

Chinese Herbal Supplement With Lead Contamination Recalled

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

May 09, 2020

FDA Warns Sellers of Essential Oils, CBD, Vitamins, and More Promoted to Treat Coronavirus

Between May 7 and May 8, 2020, the FDA issued warning letters to seven companies for selling products such as essential oils, CBD, hand sanitizers, and vitamins with unsupported claims that they can treat coronavirus (COVID-19).

April 14, 2020

Herbs of Kedem Warned for Making Coronavirus Claims

On April 10, 2020, the FDA issued a warning letter to Herbs of Kedem for selling products with unsupported claims that they can treat coronavirus (COVID-19).

March 20, 2020

Kudzu Supplement Recalled for Salmonella Risk

On March 18, 2020, Mountain Rose Herbs issued a recall of all sizes of Organic Kudzu Root Herbal Supplement because recent testing found it has the potential to be contaminated with Salmonella.

November 12, 2019

Libido Supplement for Men and Women Recalled

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

September 21, 2019

Liquid Vitamin C for Men Recalled

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

October 26, 2019

Green Lumber Enhancement Supplements Recalled

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

October 08, 2019

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

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

August 31, 2016

Recall of Dangerous Chinese Herbal Supplement Expanded

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

May 26, 2017

Herbal "Sexual Enhancement Coffee" Recalled, One Death Reported

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

August 31, 2006

Canada Advises Consumers Not To Use Adulterated Sleep Supplement

On August 30, 2006, Health Canada (the Candian Health Ministry) Health Canada advised consumers not to use Salt Spring Herbals Sleep Well Dietary Supplement because a sample analyzed by Health Canada has been found to contain the undeclared drug estazolam, a sedative that can be habit-forming when ...

April 11, 2008

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

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

August 28, 2013

Tea and Papaya Supplement Company Warned For Drug Claims

On August 12, 2013, the FDA issued a warning letter to Herbal Papaya, LLC, following a review of the company's website and Facebook page which found statements made about Papaya Seed Extract Capsules, 100% Papaya Leaf (Paw Paw Twig) and Papaya Leaf with Rooibos Tea to be drug claims. 

May 06, 2017

Herbal Teas Recalled Due To Botulism Risk

On May 1, 2017, U.S. Deer Antler Ex. & Imp. of Los Angeles, California, issued a recall of various herbal teas because they have the potential to be contaminated with Clostridium botulinum. This bacterium can cause botulism, a potentially fatal form of food poisoning.

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.

August 16, 2016

Chinese Herbal Supplement Recalled Due to Lead Contamination

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

February 13, 2016

Cannabis Compound Not Permitted in Supplements, FDA Warns

On February 4, 2016, the FDA issued warning letters to eight companies selling products containing cannabidiol (CBD), a compound derived from cannabis (also known as marijuana). In the U.S., cannabidiol is not permitted to be sold as an ingredient in dietary supplements.

July 18, 2017

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

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

April 26, 2018

Wegmans Recalls Traditional Medicinals Teas Due to Salmonella Risk

On April 17, 2018, Wegmans Food Markets issued a recall of one lot each of  Traditional Medicinals Throat Coat Lemon Echinacea herbal tea and Traditional Medicinals EveryDay Detox Lemon tea because they have the potential to contaminated with Salmonella.

May 04, 2019

High Levels of Lead Found in Chinese Herbal Supplements

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

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.

April 19, 2007

Recall of Another Sex Enhancement Supplement

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

December 14, 2003

"Herbal" Eczema Creams Found to Contain Potent Steroids

A recent British study reported that 20 of 24 creams used to treat eczema in children were found to illegally contain unlabeled amounts of corticosteroids.

September 07, 2002

FDA Sends Warning Letters to Seven Online Supplement Sellers For Therapeutic Claims

On August 27, 2002, the FDA posted seven "Cyber" letters recently issued from its Center for Food Safety and Applied Nutrition (CFSAN) to internet website operators promoting dietary supplement products that claim to diagnose, mitigate, treat, cure, or prevent a specific disease or class of ...

October 30, 2008

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

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

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.

November 04, 2016

Liver Injuries Linked With Dietary Supplement Use on the Rise

The number of liver injuries associated with dietary supplement use has increased substantially in recent years, according to a recently published study in the journal Hepatology.

March 13, 2020

State of Missouri Sues Jim Bakker Show for Selling False Coronavirus Cure

On March 12, 2020, the Missouri Attourney General announced that it sued the Jim Bakker Show for selling a fake coronavirus (COVID-19) cure called Silver Solution.

January 27, 2003

FTC Charges Dr. Clark and Related Companies with Making Unsubstantiated Health Claims

The Federal Trade Commission has charged a Switzerland-based company and its U.S. counterpart with making numerous unsubstantiated efficacy claims for a variety of dietary supplements and devices that they sell on the Internet.

January 11, 2012

Herbal Extract Company Warned by FDA of Making Drug Claims

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

June 01, 2011

FDA Finds Pesticides in Ginseng Supplement

The U.S. FDA found pesticides in Root to Health, American Ginseng, Herbal Supplement (500 Veggie Capsules, 500 mg each) according to a May 13, 2011 Warning Letter from the FDA to the manufacturer of the product, Hsu's Ginseng Enterprises, Inc.

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.

November 29, 2016

Bentonite Clay Promoted for "Detoxification" Contaminated With Lead

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

April 24, 2018

Traditional Medicinals "Throat Coat" Lemon Echinacea Herbal Tea Recalled in Canada

On April 24, 2018, Health Canada (the Canadian equivalent of the FDA) advised consumers that one lot of Traditional Medicinals Throat Coat Lemon Echinacea herbal tea is being recalled in Canada because it has the potential to contaminated by Salmonella.

July 23, 2013

Weight Loss Supplements Containing Undeclared Drugs Recalled

On July 19, 2013, Herbal Give Care LLC issued a voluntary recall of all lots of weight loss supplements Esbelin siloutte te and Esbelin siloutte Herbal Blend with L-Carnitine because they were found to contain undeclared sibutramine, N-desmethylsibutramine, and N-di-desmethylsibutramine.

January 23, 2014

Many Thyroid Supplements Contain Thyroid Hormones -- Risk of Thyrotoxicosis

A recent study found that 9 out of 10 supplements marketed for "thyroid support" and purchased at retail stores or on the Internet contained actual thyroid hormones thyroxine (T4) and/or triiodothyronine (T3), posing a risk to consumers.

October 21, 2014

Seller of Weight Loss Supplements Warned for Manufacturing Violations and Drug Claims

On October 7, 2014, the FDA issued a warning letter to YoungYou International, Inc.

August 16, 2014

FDA Warns Consumers Not To Use Herbal Sexual Enhancement Supplement

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

December 12, 2014

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

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

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 ...

November 28, 2015

Herbal Supplements Linked to Heavy Metal Poisoning

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

November 21, 2015

Ultimate Herbal Slimcaps Recalled

On November 19, 2015 Fit Firm and Fabulous issued a voluntary recall certain lots of weight loss supplement Ultimate Herbal Slimcap capsules because they were found to contain sibutramine.

September 23, 2017

Enhancement Supplement "Vegetable Vigra" Recalled

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

September 21, 2017

Sexual Enhancement Supplements Containing Prescription Drugs Recalled

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

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

August 03, 2017

AMPT "Sexual Enhancement" Coffee Recalled

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

July 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 13, 2010

Recall of Herbal Slimming Supplement Spiked with Drug

The U.S. FDA posted a notice dated August 18, 2010 indicating that Slim-30 Herbal Supplement (Lot 6032101) has been recalled by its distributor, J & H Besta Corp.

November 14, 2012

Maker of Vitamin C, Aloe and Sexual Enhancement Supplements Warned for Drug Claims and Misbranding

On October 22, 2012, the FDA issued a warning letter to Health Breakthroughs International, LLC after a review of the company's product labels and website found the dietary supplements Amazing C, MPS-Gold 100 and Power Herbal Formula to be promoted as drugs.

August 25, 2002

Canadian Recall and Stop-Sale Order on All Kava Products

Health Canada is issuing a stop-sale order for all products containing the herb kava after a safety assessment concluded there is insufficient evidence to support their safe use. The department is also requesting the recall of these products from all levels of the market.

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.

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.

January 02, 2004

Canada Reiterates Warning on Products Containing Kava

On December 23, 2003, Health Canada reminded Canadian consumers of the serious risks associated with the use of products containing kava.

December 12, 2014

Seller of B-12, Zinc, Echinacea and More Warned for Manufacturing Violations and Drug Claims

On November 14, 2014, the FDA issued a warning letter to Scientific Botanicals Company, Inc.

August 21, 2013

Seller of Vitamin, Tea and MSM Supplements Warned For Drug Claims

August 7, 2013, the FDA issued a warning letter to Vibrant Life Vitamins, following a review of the company's websites which found statements made about Taheebo Life Tea, Life Glow Plus, Super Life Glow, Life Glow Basic, Vibrant Life MSM, Herbal MSM, and Organic Germanium to be drug claims. 

May 03, 2002

More Information on Recall of PC-SPES - Prostate Supplement

The FDA's May 1, 2002 Enforcement Report classified the recall of PC-SPES as a Class I recall. The recall was originally announced by its manufacturer in February with additional warnings from the FDA issued in March (see the 3/11/02 posting on ConsumerLab.

March 11, 2002

Recall and Warning to Stop Use of Prostate Supplements "PC SPES" and "SPES"

Note: This posting was origially made on February 8, 2002. Additional information was added on March 11, 2002.

October 29, 2008

Two Vitamin C Supplements Recalled in Canada for Vitamin A Risk

On October 28, 2008, Health Canada warned Canadians, expecially expectant mothers, not to use two vitamin C products sold under the brand names New Roots Herbal Vitamin C8 and Vitazan Professional Vitamin C Advanced Ascorbate.

August 30, 2012

FDA Warns of Medical Claims Made For Numerous Chinese Herbal Products

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

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.

May 18, 2012

Caution with Butterbur Indicated by UK Warning

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

February 11, 2012

Herbal Sprays for Colds and Cold Sores Recalled

On February 10, 2012 the U.S. FDA posted a notice announcing the recall of all "Koff & Kold" and "Kold Sore" sprays by Wholistic Herbs Inc. The products were distributed throughout the United States.

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.

May 03, 2010

FDA Warns Consumers to Avoid Breath Supplement Contaminated with Lead

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

October 05, 2011

FDA Warns Herbal Nitro of Manufacturing Violations

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

June 19, 2013

Sexual Enhancement Supplement Found To Contain Undeclared Drug

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

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.

January 31, 2014

Weight Loss Supplement Containing DMAA Recalled

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

September 05, 2013

Seller of Herbal Supplements and "Tonics" Warned For Manufacturing Violations and Drug Claims

On May 24, 2013, the FDA issued a warning letter to Sundial Herbal Products following a facility inspection which found the company's products, including Woman Back Tonic, Koromantee, Wood and Root Tonic, Arthritis, Asthma, Diabetics, Sundial Ashanti Weight Loss Energy Lifter, Appetite Suppresser, ...

October 16, 2014

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

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

November 21, 2014

Herbal Arthritis Supplement Found to Contain Undeclared Drugs

On November 20, 2014, the FDA warned consumers not to purchase or use the herbal dietary supplement Feng Shi Ling because it was found to contain the undeclared drugs diclofenac and indomethacin.

November 11, 2014

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

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

November 11, 2014

Seller of Sexual, Muscle Enhancement Supplements Warned for Manufacturing Violations and Drug Claims

On August 26, 2014, the FDA issued a warning letter to GE Pharma LLC following a facility inspection which found the company's products, including Fire Burn, Fire Storm, Creatine, Amino Fire, Nitric Fire, Jet Fire, Oxy Fire, HGH, Cissus, Hydro shield, Performa-Test, Raspberry Ketones, Fire Drol, ...

October 31, 2014

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

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

October 30, 2014

Supplement Maker Warned for Manufacturing Violations

On October 21, 2014, the FDA issued a warning letter to DNG Trading & Milling, LLC, following a facility inspection which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

January 31, 2015

Maker of Soy and Zinc Warned for Manufacturing Violations

On December 18, 2014, the FDA issued a warning letter to PreMark Health Science, Inc.

January 27, 2015

Seller of Aloe, Sexual Enhancement Supplements and More Warned for Manufacturing Violations, Drug Claims

On January 8, 2015, the FDA issued a warning letter to Aloe Man, Inc., following a facility inspection which found the company's products, including The Aloe Man's Super Bright, Dr. Johnson's Maximum Desire, Dr. Johnson's Body Healer, and Dr.

January 23, 2015

Maker of Vitamin Drinks Warned for Manufacturing Violations

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

January 21, 2015

Supplement Maker Ordered to Stop Selling Products

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

January 17, 2015

Supplement Maker Warned for Manufacturing Violations

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

January 17, 2015

Maker of Magnesium and Potassium Supplements Warned for Manufacturing Violations

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

December 30, 2014

Maker of Probiotic Supplement Warned for Manufacturing Violations

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

December 30, 2014

Maker of Aloe, Weight Loss Supplements and More Warned for Manufacturing Violations, Drug Claims

On December 17, 2014, the FDA issued a warning letter to Dandy Day Corporation, following a facility inspection which found the company's products, including Aloe Pearl, Alfalo, Aloespring, Crave Away, Original Supreme Energy, Ener "G," Can G, Flora G, Flora G Plus, and Garolic, to be adulterated ...

November 18, 2015

Seller of "Hangover" Supplement Warned for Manufacturing Violations & Drug Claims

On September 17, 2015, the FDA issued a warning letter to Life Support Development Ltd, following a facility inspection which found the company's product, including Life Support Hangover Relief to be adulterated because they prepared, packed, or held under conditions that violate ...

September 09, 2015

Weight Supplement Found to Contain Drug

On September 3, 2015 the FDA warned consumers not to buy or use the weight loss supplement Meizi Super Power Fruits Herbal Slimming Formula because it was found to contain sibutramine.

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.

November 07, 2015

Power Khan Herbal Enhancement Supplement Found to Contain Drug

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

October 24, 2015

Eight Enhancement Supplements Found to Contain Undeclared Drugs

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

October 24, 2015

Drug Found in Male Enhancement Supplement

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

October 17, 2015

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

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

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 18, 2015

High Levels of Mercury and Lead Found in Ayurvedic Herbal Supplements

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

November 28, 2015

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

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

December 01, 2015

Enhancement Supplements Found to Contain Prescription Drug

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

February 09, 2016

St. John's Wort Supplements Recalled

On February 8, 2016, the Medicines and Healthcare products Regulatory Agency (MHRA) (the British equivalent of the FDA) announced that certain St. John's wort supplements are being recalled because they contain excessive levels of a toxic pyrrolizidine alkaloid (PA).

January 22, 2016

Male Enhancement Gum and Pills Contain Hidden Drug

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

December 29, 2015

Maker of Vitamin K, Vitamin A & More Warned for Manufacturing Violations, Drug Claims

On December 10 2015, the FDA issued a warning letter to Dherbs Health Emporium, Inc.

December 19, 2015

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

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

February 10, 2015

Seller of "Natural" Cough Syrup Warned for Manufacturing Violations, Drug Claims

On January 21, 2015, the FDA issued a warning letter to Fragrance Manufacturing Incorporated, following a facility inspection which found the company's products, including Maty's All Natural Cough Syrup and Maty's All Natural Cough Syrup for Kids, to be adulterated because they ...

March 10, 2015

Seller of Vision Supplements Warned for Manufacturing Violations, Drug Claims

On February 26, 2015, the FDA issued a warning letter to Biosyntrx, following a facility inspection which found the company's products, including BioTears Oral Gel Caps, ZoOmega-3 Concentrated Pharmaceutical-Grade Fish Oil, EpiCor A Nutrient-dense High Metabolite Immunogen, Sight C+ Mineral ...

February 28, 2015

Drugs Found in Male Enhancement Supplements

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

February 24, 2015

Seller of Heart, Brain and Diabetes Supplements Warned for Drug Claims

On February 6, 2015, the FDA issued a warning letter to LCW, Inc.

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.

August 11, 2015

Company Ordered to Stop Making and Selling Supplements

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

July 02, 2015

Maker of Arthritis Supplement Warned for Manufacturing Violations, Drug Claims

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

June 03, 2015

Maker of B-12 Energy Supplement Warned for Manufacturing Violations

On May 15, 2015, the FDA issued a warning letter to LiquidCapsule Manufacturing, LLC.

May 30, 2015

Seller of Supplements for Herpes, Prostate Cancer & More Warned for Drug Claims

On May 7, 2015, the FDA issued a warning letter to Strictly Health Corporation, following a review of the company's websites which found statements made about FENVIR, Prosta Pep and Tonalin brand CLA to be drug claims.

May 23, 2015

Seller of Magnesium, Calcium, Silver and More Warned for Manufacturing Violations, Drug Claims

On May 8, 2015, the FDA issued a warning letter to Pick and Pay, Inc.

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.

April 17, 2015

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

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

April 12, 2019

Sexual Enhancement Supplement for Men Recalled

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

April 08, 2019

Herbal "Coffee" for Sexual Enhancement Recalled

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

February 19, 2019

DG Baby Gripe Water Herbal Supplement Recalled

On February 15, 2019, Kingston Pharma, LLC issued a recall of all lots of DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts due to the presence of an undissolved ingredient, citrus flavonoid.

July 18, 2017

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

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

April 19, 2017

Sexual Enhancement Supplements for Men and Women Recalled

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

April 01, 2017

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 ...

March 11, 2017

Two Hospitalized After Drinking Herbal Tea With Aconite

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

July 29, 2017

Increase in Calls to Poison Control Centers About Supplements

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

May 15, 2019

Titanium 4000 Capsules for Men Recalled

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

May 07, 2019

"The Beast" Supplement for Men Recalled

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

August 05, 2017

Children's Ayurvedic Medicine Formula Contains High Levels of Lead

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

May 26, 2017

"Allergy" Supplement Containing Ephedra Recalled

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

February 21, 2017

Sexual Enhancement Supplement Recalled

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

February 09, 2017

Herbal Supplement Found to Contain Ephedra Alkaloids Recalled

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

February 07, 2017

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

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

March 09, 2016

Four Sexual Enhancement Supplements Recalled

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

March 02, 2016

Cyanide Danger With Certain Supplements, Health Canada Warns

On February 25, 2016,  Health Canada (the Canadian equivalent of the FDA) warned that a number of products which were available for sale in Canada may contain a potentially toxic compound called amygdalin.

November 28, 2014

Seller of Herbal Extracts Warned for Manufacturing Violations, Drug Claims

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

May 26, 2015

Skin Measurement Device Used to Select Nutritional Supplements Not Approved for This Use, FDA Warns

On May 8, 2015, the FDA issued a warning letter to ZYTO Technologies, Inc.

November 04, 2002

Recall Of Selected Store Brand Infant Formula in U.S.

On November 1, 2002, Wyeth Nutrition, in consultation with the U.S.

March 04, 2008

Airborne Settles Lawsuit Over False Advertising of its "Miracle Cold Buster"

On March 4, 3008, the Center for Science in the Public Interest (CSPI) announced that the makers of Airborne -- a multivitamin and herbal supplement whose labels and ads falsely claimed that the product cures and prevents colds -- will refund money to consumers who bought the product, as part of a ...

August 16, 2006

Marketers of Diabetes Supplement Banned From Claiming Products Treat or Cure Diseases

On August 10, 2006, the Federal Trade Commission (FTC) announced that an operation selling Chinese herbal supplements is banned from claiming its products treat or cure diseases, to settle FTC charges it violated a previous court order.

February 15, 2006

New Zealand Warns of Liver Toxicity from Black Cohosh

On February 9, 2006, New Zealand's Therapeutic Goods Administration (TGA) announced new labelling and consumer information for medicines containing Black cohosh (Cimicifuga racemosa).

December 22, 2005

Health Canada Warns Consumers Not to Take Chaparral

On December 21, 2005, Health Canada (Canada's health ministry) warned consumers not to ingest the herb chaparral in the form of loose leaves, teas, capsules or bulk herbal products because of the risk of liver and kidney problems.

March 10, 2015

Maker of Magnesium, Calcium, Zinc, B Vitamins and More Warned for Manufacturing Violations, Drug Claims

On January 8, 2015, the FDA issued a warning letter to Complete H2O Minerals, following a facility inspection which found the company's products, including Sulfur Concentrate, Copper, Extra Strength Copper, Extra Strength Magnesium, Extra Strength Zinc, Platinum, Gold, Indium, Molybdenum, ...

February 24, 2015

Seller of Antioxidant Water, Energy Drops Warned for Manufacturing Violations and Drug Claims

On February 18, 2015, the FDA issued a warning letter to Better Health Lab, Inc.

May 30, 2015

Seller of Omega-3, Probiotics & SuperFoods Warned for Manufacturing Violations, Drug Claims

On May 4, 2015, the FDA issued a warning letter to Dr. Dennis Black, LLC.

June 11, 2015

FDA Warns Maker of Fruit Energy Drinks for Drug Claims

On May 19, 2015, the FDA issued a warning letter to CK Management, Inc. following a facility inspection which found statements made on product labels and websites about Whole5, Fruit of the Spirit and ViaViente "whole food" fruit puree energy drinks to be drug claims.

December 16, 2015

Maker of Red Yeast Rice, St. John's Wort, Valerian and More Warned for Manufacturing Violations, Drug Claims

On December 2, 2015, the FDA issued a warning letter to Nature's Health, LLC, following a facility inspection which found the company's product, including Ginkgo & Rhodiola, Blood Sugar Balance IV, Cinnamon Extract, Choles-Balance Red Yeast Extract, Lecithin, Milk Thistle Seed Extract, ...

January 02, 2016

Fourteen Enhancement Supplements Found to Contain Undeclared Drugs

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

November 07, 2015

Seller of "NaturalDoctor" Vitamin C, Echinacea and More Warned for Manufacturing Violations

On October 16, 2015, the FDA issued a warning letter Sound Healing Arts, PC, dba Grounds for Tea, LLC, following a facility inspection which found the company's products, including  NaturalDoctor Vitamins C & K3, NaturalDoctor Goldenseal & Echinacea Plus, NaturalDoctor Centella ...

October 30, 2014

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

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

October 03, 2014

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

[Update (2/25/26): ConsumerLab was recently contacted by Saba For Life (which acquired AMS Health Sciences) requesting that this article be removed, because, in April 2016, the FDA provided AMS Health Sciences with a close-out letter ...

February 13, 2016

FDA Warns Nine Sexual Enhancement Supplements Contain Undeclared Drugs

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

November 01, 2016

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

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

May 17, 2016

Sexual Enhancement Supplement Contains Undeclared Drugs

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

July 26, 2017

Weight Loss Supplements Containing Undeclared Drug Recalled

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

February 28, 2017

Seller of Tea Supplements Warned for Manufacturing Violations

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

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.

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.

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 ...

July 15, 2014

Pinnacle Labs International Warned for Manufacturing Violations

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

July 15, 2014

Vita Springs Health Warned for Manufacturing Violations and Drug Claims

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

March 19, 2014

Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations

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

April 15, 2003

FTC Requires Scientific Evidence for "Snore Formula" Claims

On April 15 2003, the U.S. Federal Trade Commission (FTC) announced that an Arizona-based company, Snore Formula, Inc., its officers, and a distributor have agreed to settle FTC charges that they failed to have scientific substantiation for the claims made for "Dr.

January 15, 2002

Recall of "Prostatin" Supplement -- Contains Aristolochic Acid

The U.S. Food and Drug Administration (FDA) released the following Class I recall information in its January 9, 2002 Enforcement Report.

December 17, 2004

Heavy Metals Found in Some Ayurvedic Medicines

The December 15, 2004 issue of the Journal of the American Medical Association (JAMA) reported that a study of Ayurvedic herbal medicine products sold around the Boston area showed one of five products to be contaminated with one or more heavy metals (mercury and arsenic).

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.

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 ...

November 08, 2012

Chinese Herb Recalled Due To Undeclared Sulfites

On November 7, 2012, the New York State Department of Agriculture announced that Mayflower International Inc., aka Fu Xiang Yuan Trading Inc., is recalling Lily Dry after sample analysis revealed the product contains high levels of sulfites which were not declared on the label.

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.

August 31, 2012

Recent Cases of Lead Poisoning From Ayurvedic Medications from India

Public health officials have reported six cases of lead poisoning among foreign-born women who took Ayurvedic herbal products imported from India. The cases were reported by the New York City Department of Health and Mental Hygiene.

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).

January 02, 2004

Health Canada Warns Consumers Not to Use Health Products Containing Comfrey

On December 12, Health Canada advised Canadian consumers not to ingest the herb comfrey or any health products that contain comfrey because they might contain a compound called echimidine, which may cause liver damage.

March 12, 2016

FDA Finds Problems at 58% of Supplement Manufacturing Sites in U.S. and Abroad

ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2015 (ending September 30) of 483 dietary supplement manufacturing facilities, showing that most -- 58.2% -- received letters indicating noncompliance with current Good Manufacturing Practices (cGMPs).

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 ...