Showing Results for High Blood Pressure (hypertension)

10/06/2020

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.

8/17/2022

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.

4/30/2021

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 ...

12/13/2016

Case of Hemorrhagic Stroke Linked to Redline Energy Drink

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

7/06/2022

FDA Warns Kratom Companies for Arthritis, Pain Relief Claims & More

On January 30, 2022, the FDA issued warning letters to four sellers of kratom products because they were promoted to treat pain relief, opioid withdrawal, blood sugar control, anxiety, and to treat rheumatoid arthritis.

1/12/2021

Seller of Cholesterol, Weight Loss Products, and More Warned for Claims

On November 17, 2020, the FDA issued a warning letter to Bonagens following a review of the company's website, which found statements made about the company's products Anti-Aging Supports, Cholesterol & Diabetes Control, Gout Control, Hypertension Control, Liver Supports, Lungs ...

2/02/2021

FDA Warns Seller of Reishi Mushroom Supplements

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

8/17/2021

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.

3/02/2022

Seller of Holistic Tea Warned by FDA

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

3/09/2022

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).

9/12/2018

FDA Urges Consumers to Avoid Kratom

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

11/27/2018

High Levels of Lead Found in Kratom Products

Some kratom products contain levels of lead and nickel that are not considered safe for human consumption, according to tests conducted by the FDA.

12/21/2019

Supplement Company Continues to Make False Claims About Its Products, Says FTC

The FTC has filed a motion of contempt against two supplement companies that, according to the motion, have continued to promote their products with false claims despite being barred from doing so by a previous court order.

12/15/2020

FDA Warns Seller of Evening Primrose Oil and Beta Glucan

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

11/24/2020

Recalled Vitamin D Contains Potentially Dangerous Ingredient

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

12/17/2020

FTC Crackdown on Six Deceptive CBD Products

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

12/22/2021

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

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

5/11/2022

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.

10/04/2017

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

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

4/21/2020

Life Force Warned for Colloidal Silver, Nitric Oxide Claims

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

8/11/2022

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).

1/17/2018

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.

5/04/2019

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.

1/28/2020

Weight Supplement Contains Hidden Drug

On January 13, 2020, the FDA issued a warning letter to Wave Miami, LLC because the company's weight loss supplement, Lipro Dietary Capsule was found to contain the prescription medication tadalafil.

6/16/2020

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

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

4/27/2022

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

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

9/07/2016

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

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

11/06/2014

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 ...

8/06/2016

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

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

8/01/2017

"Man of Steel" Sexual Enhancement Supplements Recalled

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

11/24/2018

Dangerous Drug In Supplements for Pain and Anxiety

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

10/01/2019

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.

7/06/2021

CBD Products Were Promoted to Treat Cancer and Alzheimer's Without Proof, Says FTC

On July 6, 2021, the Federal Trade Commission (FTC) announced that it has approved a final administrative consent orders against Kushly Industries LLC and the company's owner, Cody Alt, for allegedly making unsupported health claims about its CBD products.

5/24/2021

U.S. Marshals Seize $1.3 Million Worth of Kratom

U.S. Marshals have seized approximately $1.3 million worth of bulk kratom and kratom supplements manufactured by Atofil, LLC, a subsidiary of Premier Manufacturing Products, according to the FDA.

5/08/2021

Seller of Immune Bio Green Cell Warned by FDA

On March 30, 2021, the FDA issued a warning letter to Immune & Genetics Protocols, LLC following a review of the company's websites, which found statements made about the company's product Immune Bio Green Cell to be drug claims.

3/09/2021

CBD Seller Warned for Drug and COVID-19 Claims

On March 1, 2021, the FDA issued a warning letter to Cannafyl following a review of the company's website, which found statements made about the company's products Balance CBD Drops, Relief CBD Drops, Relax CBD Drops and Relief CBD Salve to be drug claims.

3/05/2021

FTC Takes Further Action Against Deceptive CBD Claims

On March 5, 2021, the Federal Trade Commission (FTC) announced that it has approved final administrative consent orders against six companies for selling CBD products with unsupported and deceptive health claims that they can treat a variety of conditions, including cancer, heart disease, ...

10/10/2003

Government Stops Sale of Supplements Claiming to Treat Obesity and Impotence

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

6/23/2003

FDA Warns Consumers Against Taking 6 Sexual Enhancement Supplements

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

7/10/2020

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.

6/30/2020

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

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

10/18/2017

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.

1/29/2019

Prescription Drugs Found in Four Weight Loss Supplements

On January 28, 2019, the FDA the FDA warned consumers not to buy or use the following weight loss supplements because they were found to contain sibutramine and/or phenolphthalein:

• Slim Bio Capsules were found to contain sibutramine, N-desmethylsibutramine, ...

3/30/2019

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.

8/30/2012

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.

10/31/2017

Black Licorice Can Cause Abnormal Heart Rhythms, FDA Warns

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

9/09/2018

Higenamine -- A Potentially Dangerous Stimulant -- Found in Some Supplements

A recent study found concerningly high doses of the stimulant higenamine in some weight loss, energy and sports supplements sold in the U.S. Higenamine is a naturally-occurring stimulant which is permitted to be sold as a dietary supplement ingredient in the U.S.

3/06/2019

FDA Warns Consumers Not to Use Certain Sexual Enhancement Supplements

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

1/22/2019

FDA Warns Consumers Not to Use "The Silver Bullet"

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

1/13/2019

Sexual Enhancement Supplement Recalled

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

12/11/2018

Sexual Enhancement Supplement Found to Contain Prescription Drug

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

12/01/2018

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

10/16/2018

Weight Loss Supplement Containing Hidden Drug Recalled

On October 15, 2018, Fat Burners Zone issued a recall of one lot of its Zero Xtreme weight loss supplement because it was found to contain sibutramine.

7/31/2018

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.

2/02/2018

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

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

4/12/2019

CDC: Kratom Linked to 91 Deaths

Kratom may have played a role in twice as many deaths as has been previously estimated, according to a report issued today by the Center of Disease Control (CDC).

8/30/2012

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, ...

7/29/2017

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.

8/05/2017

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. 

11/08/2016

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.

10/04/2016

Turmeric Spice Recalled Due to Elevated Lead Levels

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

11/29/2016

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.

4/04/2017

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.

7/10/2017

Bodybuilding Supplements Containing Steroid-Like Substances Recalled

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

4/17/2018

Sexual Enhancement Supplement Recalled

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

4/14/2018

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.

10/18/2017

Total Body Nutrition Warned for Banned Stimulant in Supplements

On September 28, 2017, the FDA issued a warning letter to Total Body Nutrition following a facility inspection which found some of the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

2/27/2018

Weight Loss Supplement Containing Undeclared Drug Recalled

On February 27, 2018, Bella All Natural recalled their "Diet Capsules" because they contain sibutramine. 

6/22/2011

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

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

10/21/2014

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.

5/30/2014

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

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

5/17/2012

FDA Warns of Drug Ingredients in Three Sexual Enhancement Supplements

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

4/21/2012

FDA Finds Prescription Drug Analog in 3 Enhancement Supplements

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

4/03/2012

"France T253" Enhancement Supplement Contains Hidden Drug

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

1/24/2013

Food for Health Warned for Manufacturing Violations and Drug Claims on Supplements

On October 5, 2012, the FDA issued a warning letter to Food for Health International, LLC following a facility inspection which found the company's products, including Activz brand Vitamin D, Potassium Iodine, Organic Vitamin C, Whole 9 (a fruit and vegetable meal replacement shake) Control and VMA ...

9/13/2010

Supplement for "Increasing Desire" Recalled for Containing Drug

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

7/20/2010

Recall of ED Supplement Containing Drug

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

4/08/2010

Capsule for Men Spiked with Erectile Drug

On April 7, 2010, the U.S.

7/23/2009

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.

1/11/2012

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.

11/28/2015

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.

2/06/2018

FDA Links 44 Deaths to Kratom

On February 6, 2018, FDA announced it is now aware of 44 deaths associated with the use of kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms. This is an increase from the 36 deaths associated with kratom that the agency reported in November 2017.

11/14/2017

36 Deaths Associated With the Use of Kratom Products

On November 14, 2017, FDA Commissioner Scott Gottlieb, M.D. issued a statement on the dangers of using products containing kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms.

9/19/2018

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.

3/13/2018

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 ...

5/29/2003

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

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

4/09/2003

Recall of Dangerous Sexual Enhancement Supplement Illegally Containing Viagra Ingredient

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

2/07/2012

Drug-Laced Supplements and Drink Mixes Recalled

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

3/08/2012

Rx Drugs Found in Weight Loss and Enhancement Supplements

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

2/24/2011

Recall of Counterfeit Extenze Tablets Containing Drugs

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

7/13/2012

Alistrol Health Inc. Warned Over Health Claims on Products

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

4/16/2014

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

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

11/06/2014

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.

4/01/2004

Aloe Producer Recalls Product Due to Toxic Levels of Vitamin D

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

10/24/2015

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): 

8/08/2016

Turmeric Spice Recall Expanded to Include More Brands

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

7/29/2016

Ground Turmeric Spice Recalled Due to Lead Contamination

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

11/11/2015

Consuming a Single Energy Drink May Increase Cardiovascular Risk

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

8/15/2017

Protein Supplements Can Be Dangerous in People with Rare Genetic Disorder

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

7/18/2017

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.

8/03/2017

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. 

9/23/2017

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. 

7/26/2017

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.

3/25/2008

FDA Warns of Sexual Supplements with Drug-like Ingredients

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

5/10/2007

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.

11/26/2007

Encore Tabs Recalled -- Contain Prescription Drug

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

3/04/2008

Two Supplements Recalled for Containing Viagra-like Compounds

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

5/29/2008

Recall of Virility Supplement

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

11/03/2004

FDA Warns of Sexual Enhancement Supplements Containing Prescription Drug

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

3/20/2007

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.

7/30/2008

Recall of Viapro Capsules Due to Potentially Harmful Ingredient

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

4/07/2010

Nationwide Recall of Masxtreme Capsules Containing Drugs with Cardiovascular Side Effects

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

12/14/2009

Nationwide Recall of Sexual Enhancement Supplements Containing Drug-like Compound

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

9/12/2010

Mr. Magic Male Enhancer Recalled

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

8/13/2010

Recall of Male Enhancement Supplement Sold in National Stores

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

4/29/2014

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

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

1/01/2011

Recall of Two Supplements Spiked with Erectile Dysfunction Drug

On December 22, 2010 the U.S.

2/16/2012

Recall of Enhancement Supplement for Women -- Contains Drug

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

3/02/2012

Recall of Enhancement Supplement for Men -- Contains Drug

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

7/19/2011

Recall of Enhancement Supplement for Men - Contains Drug Compounds

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

5/06/2015

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.  

9/18/2012

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

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

10/24/2012

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

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

1/18/2003

Non-Prescription Anti-Hypertension Pills Recalled

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

9/13/2010

ExtenZe Enhancement Supplements Seized in Canada

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

3/28/2011

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

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

3/09/2016

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.

12/12/2015

Sexual Enhancement Supplement Recalled

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

8/05/2016

More Turmeric Spice Recalled

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

8/31/2016

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.

8/16/2016

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.

6/06/2017

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

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

2/09/2017

Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products

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

11/25/2016

DMAA Product Recalled

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

7/20/2017

Jail Time for Seller of Spiked Supplements

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

7/18/2017

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.

11/02/2012

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.

12/08/2009

Warning on Acai Berry Supplements Spiked with Drug

On December 8, 2009, Health Canada (the Canadian health agency) advised consumers not to use certain Acai Berry products after a large number of shipments of adulterated products were stopped at the border.

7/29/2008

Recall of Sexual Enhancement Supplements Containing Drug

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

6/15/2009

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

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

7/13/2006

FDA Warns About Sexual Enhancement Supplements with Dangerous Ingredients

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

5/28/2008

FDA Requests Recall of Xiadafil VIP Supplements

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

12/30/2007

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

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

4/19/2007

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.

8/30/2006

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

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

4/07/2011

Prostate Drug Found in Prostate Supplement -- Recall Underway

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

11/21/2012

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

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

9/18/2015

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.

12/21/2012

Dangerous Supplement Being Sold Under New Name

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

6/04/2012

FDA Warning on Supplement for Pain Relief

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

10/30/2008

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.

11/26/2012

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

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

9/30/2015

Weight and Energy Supplement Contains Synthetic "Amphetamine"

On September 21, 2015, the FDA issued a warning letter to TruVision Health LLC. because the company's supplement tru Weight & Energy lists a synthetic, amphetamine-like compound, AMP (also called 1,3-dimethylbutylamine or DMBA) on product labels. 

10/24/2015

Four Weight Loss Supplements Found To Contain Drugs

On October 23, 2015, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain sibutramine, phenolphthalein and/or sildenfil. Each was identified during an examination of international mail shipments:

5/02/2016

Weight Loss Supplements Containing Hidden Drugs Recalled

On April 29, 2016 Making It A Lifestyle, L.L.C. issued a recall of all lots of weight loss supplements 3rd Degree, Black Gold X Advanced and Black Label X because they were found to contain undeclared sibutramine and sildenafil.

4/08/2016

Large Doses of Stimulant Methylsynephrine Found In Weight Loss Supplements

Amounts of methylsynephrine found in some supplements exceed prescription dosages, according to new study published in Drug Testing and Analysis.

3/20/2016

FDA Warns of Weight Supplements Containing Undeclared Drugs

On March 17, 2016, the FDA warned consumers not to buy or use the weight loss supplements listed below because they were found to contain undeclared drugs:

7/25/2015

Weight Supplement Found to Contain Three Drugs

On July 23, 2015 Life & More, L.L.C. issued a voluntary recall of 783 bottles from one lot of Akttive High Performance Fat Burner Gold weight loss capsules because they were found to contain the undeclared drugs sibutramine, desmethylsibutramine, and phenolphthalein.

3/19/2007

Canada Warns of Weight Loss Supplement with Rx Drug

On March 14, 2007, Health Canada advised consumers not to use MIAOZI Slimming Capsules because they have been found to contain sibutramine, a prescription medication that should only be taken under medical supervision.

4/17/2015

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.

11/14/2014

FDA Warns Consumers Not to Buy or Use Muscle Enhancement Supplement

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

7/24/2014

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

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

2/20/2013

Recall: Arthritis and Muscle Pain Supplement Contains Prescription Drugs

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

10/15/2007

US Marshalls Seize Charantea Supplements Promoted for Diabetes, Anemia and Hypertension

At the request of the U.S. Food and Drug Administration (FDA), on October 9, 2007, U.S. Marshals seized approximately $71,000 of goods from FulLife Natural Options, Inc., of Boca Raton, Fla., which marketed and distributed Charantea Ampalaya Capsules and Charantea Ampalaya Tea.

2/13/2013

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

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

12/14/2010

FDA Warns Consumers to Avoid Man Up Now Capsules

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

10/08/2010

FDA Warns of Stimulant in Slimming Capsules

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

3/29/2013

Prescription Drugs Found In Prostate and Sexual Enhancement Supplements

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

5/17/2016

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.

9/27/2016

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

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

9/02/2016

Kratom To Be Classified a Schedule I Controlled Substance

On August 30, 2016, the U.S. Drug Enforcement Agency (DEA) announced its intent to classify the active compounds (mitragynine and 7-hydroxymitragynine) in kratom as Schedule I controlled substances.  

8/08/2014

FDA Warns Puerto Rico Supplement Seller

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

2/07/2013

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

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

1/30/2013

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

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

8/28/2008

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

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

7/28/2008

Seizure of Xiadafil VIP Tablets After Company Refuses Recall

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

10/17/2012

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.

8/22/2012

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

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

9/13/2014

Three Weight Loss Supplements Found to Contain Drugs

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

9/13/2013

Metagenics Warned For Misbranding of Medical Foods and Drug Claims

On August 13, 2013, the FDA issued a warning letter to Metagenics, Inc.

8/01/2013

Maker of Algae Products Warned For Drug Claims, Manufacturing Violations

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

11/06/2009

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

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

2/15/2013

FDA Seizes Weight Loss Supplements Containing Undeclared Drug

On Feb. 14, 2013, U.S. Marshals acting on behalf of the FDA seized weight loss supplements from Globe All Wellness, LLC which were found to contain the undeclared drug sibutramine hydrochloride.

11/07/2013

FDA Warns Consumers of Weight Loss Supplement Containing Multiple Drugs

On November 7, 2013, the FDA warned consumers not to buy or use Jimpness Beauty Fat Loss Capsules because they were found to contain sibutramine, phenolphthalein, and sildenafil.

5/24/2013

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.

2/26/2015

Weight Loss Supplement Found to Contain Multiple Drugs

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

2/22/2012

"Japan Weight Loss Blue" Pills Dangerous According to FDA

On February 18, 2012, the U.S. Food and Drug Administration (FDA) advised consumers not to purchase or use “Japan Weight Loss Blue,” a product for weight loss sold on various websites, including www.vitaminbestbuy.com.

3/13/2015

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.

8/01/2013

Fat Loss and Muscle Enhancement Supplements Found To Contain DMAA

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

12/22/2008

FDA Warns Consumers About Tainted Weight Loss Pills

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

11/25/2007

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 ...

3/13/2015

Three Weight Loss Supplements Found to Contain Drugs

The FDA recently warned consumers not to buy or use the following weight loss supplements because they were found to contain undeclared drugs. Each was identified during an examination of international mail shipments.

8/07/2015

Male Enhancement and Weight Loss Supplement Containing Drugs Recalled

On August 6, 2015 Blue Square Market Inc. issued a recall of the following supplements which were found to contain undeclared drugs:

4/04/2013

Three More Sexual Enhancement Supplements Found To Contain Undeclared Drugs

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

2/24/2015

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.

6/25/2014

More Generic Versions of Heart Medication Recalled

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

2/01/2012

FDA Warns Seller of Almased Weight Loss Product of Marketing Violations

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

8/31/2012

Energy, Fat Loss Supplement Recalled For Ephedrine Alkaloids

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

11/08/2012

FDA Warns Consumers of "Slimming Coffee"

On November 8, 2012, the FDA warned consumers not to purchase or use Best Share Green Coffee: Brazilian Slimming Coffee after FDA testing revealed the coffee, which was promoted for weight loss, contains the drug sibutramine.

11/28/2008

Fat Loss Supplement Recalled for Containing Prescription Drug

On November 26, 2008, the FDA reported that Zhen De Shou Fat Loss Capsules are being recalled by the distributor, Fashion Sanctuary. FDA analysis found the product to contain undeclared sibutramine, an FDA approved drug used as an appetite suppressant for weight loss.

4/23/2009

Recall of "Slimming" Supplements Spiked with Drug

On April 20, 2009 the U.S. FDA reported a nationwide recall of dietary supplements distributed by Universal ABC Beauty Supply International.

9/13/2010

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.

8/11/2008

Stroke Attributed to Xenadrine Ephedra-Free Supplement

A case report in the journal Military Medicine (July 2008) attributes the occurance of vasospasm and stroke in a 36 year-old women to use of Xenadrine-EFX, a supplement used for weight loss.

10/27/2004

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

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

4/11/2013

Glutathione Supplement Maker Warned For Manufacturing Violations and Drug Claims

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

9/27/2013

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

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

9/15/2013

Creatine Powder Containing DMAA Recalled

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

7/24/2013

USPLabs Destroys $8 Million Worth of Supplements Containing DMAA

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

6/23/2013

Weight Loss Supplements Containing DMAA Recalled

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

1/31/2014

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.

11/20/2013

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

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

8/08/2014

Weight Loss Supplement Found to Contain DMAA Recalled

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

9/02/2014

Recall of Weight Loss Supplement Expanded

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

10/10/2014

Weight Loss Supplement Found to Contain Multiple Drugs

On October 10, 2014, the FDA warned consumers not to purchase or use the dietary supplement Japan Hokkaido Slimming Weight Loss Pills because it was found to multiple contain undeclared drugs, including sibutramine, phenolphthalein, benzocaine and diclofenac.

9/12/2012

Distribution of Weight Loss Product Containing DMAA Should Be Stopped Immediately, Warns FDA

On August 28, 2012, the FDA issued a warning letter to Regeneca stating that the company's RegeneSlim, which was promoted as a dietary supplement for weight loss, is adulterated with dimethylamylamine (DMAA) and that failure to immediately cease distribution of this product could result in FDA ...

10/03/2014

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

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