Product Reviews and Information for Sexual Enhancement
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Product Review
Sexual Enhancer Supplements Review (with Yohimbe, Horny Goat Weed, Arginine)
Choose the Best Sexual Enhancer Supplement. Only 30% of Selected Sexual Enhancement Supplements Pass Quality Tests.
CL Answer
Is it safe to take arginine, or other supplements for sexual enhancement, while taking Viagra or Cialis?
When taking Cialis or Viagra, is it safe to take arginine or other sexual enhancement supplements?
Product Review
L-Arginine Supplements Review
Choose the Best L-Arginine Supplement. Find Out Which L-Arginine Supplement Passed CL's Tests.
CL Answer
Which supplements help with erectile dysfunction?
Supplements for erectile dysfunction. Find out which supplements can help with ED, including ginseng, L-arginine, and maca.
News Release
July 22, 2015
ConsumerLab.com Tests DHEA Supplements, Warns of Differences in Dose and Price
White Plains, New York, July 22, 2015 — DHEA is a controversial hormone supplement touted for anti-aging effects — but what can it really do? ConsumerLab.com reviewed the evidence and purchased many popular brands of DHEA to test their quality.
Recalls & Warnings
January 24, 2015
FDA Warns Consumers Not To Use Sexual Enhancement Supplement
On January 21, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Happy Passengers, because it was found to contain undeclared sildenafil. Sildenafil, the active ingredient in Viagra, which is prescribed for erectile dysfunction.
Recalls & Warnings
December 26, 2014
Three Sexual Enhancement Supplements Found to Contain Hidden Drugs
On December 23, 2014, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain an undeclared drug.
Recalls & Warnings
January 04, 2015
Sexual Enhancement Supplement Recalled
On December 30, 2014, Vivo Brand Management (Canada) issued a recall of one lot of the sexual enhancement supplement Forta for Men, because it was found to contain undeclared homosildenafil.
Recalls & Warnings
August 20, 2014
Sexual Enhancement Supplement Contains Hidden Drug
On August 11, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement Arize because it was found to contain sulfoaildenafil. Sulfoaildenafil is structurally similar to sildenafil, the active ingredient in Viagra, which is prescribed for erectile dysfunction.
Recalls & Warnings
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.
Recalls & Warnings
July 23, 2014
Sexual Enhancement Supplement Found to Contain Hidden Drug
On July 22, 2014, the FDA warned consumers not to buy or use sexual enhancement supplement O.M.G. because it was found to contain sildenafil.
Recalls & Warnings
May 29, 2014
Recall of Sexual Enhancement Supplements Expanded
On May 28, 2014, Eugene Oregon, Inc. expanded its previous recall of certain lots of sexual enhancement supplements African Black Ant, Black Ant, and Mojo Risen. All lots of these supplements are now recalled.
Recalls & Warnings
May 16, 2014
Sexual Enhancement Supplement Contains Hidden Drug
On May 16, 2014, the FDA warned consumers not to buy or use sexual enhancement supplement MV5 Days because it was found to contain sildenafil.
Recalls & Warnings
May 07, 2014
Three Sexual Enhancement Supplements Recalled
On May 5, 2014 , Eugene Oregon, Inc. issued a precautionary, voluntary recall of sexual enhancement supplements African Black Ant, Black Ant and Mojo Risen.
Recalls & Warnings
April 18, 2014
Sexual Enhancement Supplement Contains Undeclared Drug
On April 16, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement S.W.A.G because it was found to contain sildenafil.
Recalls & Warnings
June 06, 2014
Sexual Enhancement Supplement Found to Contain Drug
On June 5, 2014, the FDA warned consumers not to buy or use sexual enhancement supplement Zhen Gong Fu because it was found to contain sildenafil.
Recalls & Warnings
March 31, 2014
Seven Sexual Enhancement Supplements Recalled Due to Undeclared Drugs
On March 27, 2014, Nova Products, Inc. issued a voluntary recall of sexual enhancement supplements African Black Ant, Black Ant, XZen Gold, ZXen Platinum, XZen 1200, XZone Gold and XZone 1200.
Recalls & Warnings
January 14, 2014
Seven Sexual Enhancement Supplements Containing Undeclared Drugs Recalled
On January 9, 2014, Midwest Wholesale issued a voluntary recall of seven sexual enhancement supplements: Boost Ultra, XZone Gold, Sexy Monkey, Triple MiracleZen Platinum, Magic for Men, "New" Extenze, and New XZen Platinum.
Recalls & Warnings
December 20, 2013
Two Sexual Enhancement Supplements Found to Contain Undeclared Drugs
On December 19, 2013, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared sildenafil or drugs chemically similar to sildenafil:
Recalls & Warnings
July 26, 2022
Sexual Enhancement Supplement Sold on Amazon Recalled
On July 21, 2022, Ultra Supplements LLC issued a recall of one lot of Sustango capsules after Amazon laboratory analysis found the presence of the prescription drug Tadalafil. The company has received no reports of adverse effects related to this recall to date.
Recalls & Warnings
March 07, 2014
Sexual Enhancement Supplement Found to Contain Undeclared Drug
On March 7, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplement Weekend Warrior because it was found to contain undeclared thiosildenafil.
Recalls & Warnings
June 18, 2014
Two Sexual Enhancement Supplements Found to Contain Drug
On June 17, 2014, the FDA warned consumers not to buy or use the sexual enhancement supplements listed below because they were found to contain sildenafil.
Recalls & Warnings
March 02, 2015
Four More Sexual Enhancement Supplements Found To Contain Hidden Drug
On March 2, 2015, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
March 02, 2015
Hidden Drug Found in Six Sexual Enhancement Supplements
On February 27 and February 28, 2015, the FDA warned consumers not to buy or use the following six sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
March 06, 2015
Nine Male Enhancement Supplements Found to Contain Drugs
On March 2 and March 3, 2015, the FDA warned consumers not to buy or use the following nine male sexual enhancement supplements because they were found to contain an undeclared sildenafil or vardenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
October 01, 2013
Three Sexual Enhancement Supplements Containing Undeclared Drug Recalled
On September 24, 2013, Haute Health, LLC issued a voluntary recall of all lots of sexual enhancement supplements Virilis Pro, PHUK and Prolifta, because they were found to contain sildenafil.
Recalls & Warnings
September 03, 2013
Sexual Enhancement Supplements Containing Undeclared Drug Recalled
On August 27, 2013, Hardmenstore.com issued a voluntary recall of sexual enhancement supplements 72HP, Evil Root and Pro Power Max because they were found to contain undeclared sildenafil.
Recalls & Warnings
August 03, 2022
Sexual Enhancement Supplement Recalled Due to Sildenafil
On August 1, 2022, DISTRIBUTOR RFR, LLC recalled one lot of SANGTER Energy Supplement 3000 mg to the consumer level after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.
Recalls & Warnings
July 13, 2022
FDA Warns Sellers of Tainted Honey-Based Sexual Enhancement Products
On July 12, 2022, the FDA issued warning letters to four companies selling honey-based products promoted for sexual enhancement after tests conducted by the FDA found the products to contain the prescription drugs Tadalafil and Sildenafil.
Recalls & Warnings
July 15, 2022
Honey-Based Enhancement Supplement Recalled
On July 13, 2022, Shopaax.com issued a recall of all lots of its honey-based sexual enhancement product, Kingdom Honey Royal Honey VIP, after FDA analysis found the presence of undeclared sildenafil.
Recalls & Warnings
September 29, 2022
Sexual Enhancement Supplement Sold on Amazon and Walmart Recalled Due to Undeclared Drugs
On September 27, 2022, Proper Trade LLC/My Stellar Lifestyle recalled two lots of Wonder Pill after Amazon laboratory analysis found the product to contain undeclared tadalafil, a prescription medication.
Recalls & Warnings
November 17, 2022
FDA Warns Consumers Not to Use Male Enhancement Supplement
On November 10, 2022, the FDA warned consumers not to buy or use Sangter Natural Male Energy Supplement after FDA laboratory analysis confirmed the presence of undeclared sildenafil.
Recalls & Warnings
January 30, 2014
Five Sexual Enhancement Supplements Found to Contain Prescription Drugs
On January 28, 2014, the FDA warned consumers not to buy or use the five sexual enhancement supplements listed below because they were found to contain sildenafil and/or tadalafil.
Recalls & Warnings
June 04, 2014
Six Sexual Enhancement Supplements Found to Contain Hidden Drugs
On June 2, 2014, the FDA warned consumers not to buy or use the six sexual enhancement supplements listed below because they were found to contain undeclared sildenafil and tadalafil, or other drugs which are chemically similar.
Recalls & Warnings
September 27, 2013
Sexual Enhancement Supplement Containing Undeclared Drug Recalled
On September 24, 2013, the FDA warned consumers not to buy or use sexual enhancement supplement Wood-E because it was found to contain sildenafil. Sildenafil, the active ingredient in the prescription drug Viagra, is typically prescribed for erectile dysfunction.
Recalls & Warnings
November 08, 2013
Sexual Enhancement Supplement Found To Contain Prescription Drugs
On November 8, 2013, the FDA warned consumers not to purchase or use sexual enhancement supplement Vitalikor Fast Acting because it was found to contain sildenafil and vardenafil.
Recalls & Warnings
November 20, 2013
Another Sexual Enhancement Supplement Recalled Due To Undeclared Drugs
On November 18, 2013, Fossil Fuel Products, LLC issued a voluntary recall of sexual enhancement supplement RezzRX because it was found to contain the undeclared drugs hydroxylthiohomosildenafil and aminotadalafil.
Recalls & Warnings
January 11, 2023
Male Sexual Enhancement Supplement Found to Contain Prescription Drug
On January 9, 2022, the FDA issued a warning letter to Distributor RFR, LLC after laboratory analysis of the company’s SANGTER Natural Male Energy Supplement found the product to contain undeclared sildenafil, a prescription medication.
Recalls & Warnings
January 19, 2023
Male Sexual Enhancement Supplement Adam’s Secret Found to Contain Prescription Medication
On January 10, 2023, the FDA issued a warning letter to HIS Enterprise Inc dba Adam’s Secret USA, LLC after laboratory analysis found Adam’s Secret Extra Strength 3000 Platinum, Adam’s Secret Extra Strength Blue, Adam’s Secret Extra Strength Purple, Adam's Secret ...
Recalls & Warnings
July 26, 2023
Gadget Island, Inc. Male Enhancement Supplements Found to Contain Prescription Drugs
On July 21, 2023, the FDA issued a warning letter to Gadget Island, Inc.
Recalls & Warnings
March 06, 2019
FDA Warns Consumers Not to Use Certain Sexual Enhancement Supplements
On January 28, 2019, the FDA warned consumers not to buy or use the following sexual enhancement supplements were found to contain undeclared sildenafil and/or tadalafil.
Recalls & Warnings
January 22, 2019
FDA Warns Consumers Not to Use "The Silver Bullet"
On January 10, 2019, the FDA warned consumers not to buy or use the sexual enhancement supplement The Silver Bullet because it contains undeclared sildenafil and tadalafil.
Recalls & Warnings
January 13, 2019
Sexual Enhancement Supplement Recalled
On January 8, 2019, Happy Together, Inc. issued a recall of the sexual enhancement supplement Rhino 5k because FDA analysis found it to contain undeclared sildenafil and tadalafil.
Recalls & Warnings
December 11, 2018
Sexual Enhancement Supplement Found to Contain Prescription Drug
On December 10, 2018, the FDA warned consumers that the sexual enhancement supplement On Demand contains undeclared sildenafil.
Recalls & Warnings
December 01, 2018
Sexual Enhancement Supplements Contain Prescription Drugs
The FDA recently warned consumers that the following sexual enhancement supplements were found to contain undeclared sildenafil and/or tadalafil. Use the links below to read the complete warning letter for each:
- Willy Go Wild
News Release
July 01, 2015
Tests of Maca "Enhancement" Supplements Find Real Maca, But Some Lead Contamination and Seemingly Excessive Amounts of Rice Filler
White Plains, New York, July 1, 2015 — It's touted for increasing stamina and sexual performance and sales have steadily increased for more than a decade, but do maca supplements really contain this root indigenous to Peru? To answer this question, ConsumerLab.
Recalls & Warnings
November 21, 2013
Sexual Enhancement Supplement Found To Contain Multiple Drugs
On November 21, 2013, the FDA warned consumers not to buy or use sexual enhancement supplement Alpha Male because it was found to contain multiple undeclared drugs, including aminotadalafil, sulfosildenafil, sulfoaildenafil, hydroxythiohomosildenafil, dimethylsildenafil, and sildenafil.
Recalls & Warnings
November 20, 2013
Three Sexual Enhancement Supplements Recalled
On November 16, 2013, Jobbers Wholesale issued a voluntary recall of sexual enhancement supplements Rhino 5 Plus, Maxtremezen, and Extenzone because they were found to contain the undeclared drugs desmethylcarbondenafil and dapoxetine.
Recalls & Warnings
November 20, 2013
Two Sexual Enhancement Supplements Found To Contain Undeclared Drugs
On November 19, 2013, Tendex issued a voluntary recall of one lot each of sexual enhancement supplements P-Boost and NatuRECT because they were found to contain tadalafil.
Recalls & Warnings
October 30, 2013
Three Sexual Enhancement Supplements Found to Contain Prescription Drugs
On September 24, 2013, the FDA advised consumers not to purchase or use sexual enhancement supplements Xzen 1200, Xzen Gold and Xzen Xpress because they have been found to contain undeclared prescription drugs.
Recalls & Warnings
August 23, 2013
Sexual Enhancement Supplement Containing Undeclared Drugs Recalled
On August 12, 2013, Jack Rabbit Inc. issued a voluntary recall of one lot of sexual enhancement supplement Jack Rabbit because it was found to contain undeclared sildenafil and tadalafil.
Recalls & Warnings
July 22, 2013
Sexual Enhancement Supplements Containing Undeclared Drugs Recalled
On July 18, 2013, Volcano Company issued a voluntary recall all lots of Volcano Male Enhancement Liquid and Volcano Male Enhancement Capsules because they were found to contain undeclared desmethyl carbodenafil, dimethylsildenafil, and dapoxetine.
Recalls & Warnings
July 15, 2013
Two Sexual Enhancement Supplements Recalled
On July 5, 2013, Hardmenstore.com issued a voluntary recall of 430 lots of sexual enhancement supplements Silver Sword and Clalis because they were found to contain undeclared sildenafil.
Recalls & Warnings
June 28, 2013
Three Sexual Enhancement Supplements Found Contain Undeclared Drugs
On June 27, 2013, the FDA warned consumers not to buy or use MVP Mega, Exten 1300 and MaxTreme Zen, dietary supplements for sexual enhancement which were found to contain undeclared tadalafil or a combination of tadalafil and sildenafil.
News Release
January 15, 2014
Problems Found with the Quality and Labeling of Some "Muscle Enhancement" Supplements -- Review of Creatine and Branched-chain Amino Acid Supplements Published by ConsumerLab.com
White Plains, New York, January 15, 2014 — Athletes often turn to supplements such as creatine and branched-chain amino acids (BCAAs) to enhance muscle strength and recovery. These supplements may also benefit people with muscular diseases and those recovering from knee surgery.
Recalls & Warnings
November 07, 2024
Sexual Enhancement Supplements Sold on Amazon Recalled
On November 4, 2024, four sexual enhancement supplements sold on Amazon and other websites, ZoomMax and ZapMax (Boulla LLC) and VitalityXtra and PeakMax (VitalityVita LLC) were recalled because they were found to contain undeclared prescription drugs, ...
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
March 21, 2024
Eleven Brands of Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs
On March 19, 2024, Pyramid Wholesale issued a recall of 11 brands of sexual enhancement supplements, including honey-based products, after they were found to contain undeclared sildenafil and tadalafil.
Recalls & Warnings
April 03, 2024
ForeverMen Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs
On February 12, 2024, ForeverMen issued a recall of all lots of ForeverMen capsules, which are promoted for sexual enhancement, after FDA analysis found the capsules to contain undeclared sildenafil and tadalafil.
Recalls & Warnings
June 12, 2024
Integrity Enhancement Supplements for Men Recalled Due to Undeclared Prescription Drugs
On February 1, 2024, Integrity Products issued a recall of one lot of Ram It & To The Moon products, which are promoted for sexual enhancement, after FDA analysis found the capsules to contain undeclared sildenafil and tadalafil.
CL Answer
I have low blood pressure. Are there any supplements I should avoid?
Find out which supplements can cause decreases in blood pressure, including melatonin, arginine, magnesium, and calcium.
Recalls & Warnings
June 27, 2013
Another Sexual Enhancement Supplement Found Contain Undeclared Drug
On June 27, 2013, the FDA warned consumers not to buy or use Silver sword, a dietary supplement for sexual enhancement which was found to contain undeclared sildenafil.
Recalls & Warnings
May 07, 2013
FDA Warns Consumers Of Three More Sexual Enhancement Supplements Containing Undeclared Drugs
On May 7, 2013, the FDA issued a warning to consumers, urging them not to purchase or use three sexual enhancement products which were found to contain undeclared drugs.
Recalls & Warnings
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.
Recalls & Warnings
June 13, 2013
FDA Warns Consumers of Sexual Enhancement Supplements Containing Prescription Drugs
On June 10, 2013, the FDA warned consumers that a number of sexual enhancement supplements have been found to contain undeclared drugs such as sildenafil and tadalafil.
Recalls & Warnings
May 04, 2023
PrimeZEN Enhancement Supplement for Men Found to Contain Prescription Drug
On April 27, 2023, the FDA issued a warning letter to Tager Online, Inc. DBA Volt Candy; Volt Candy Wholesale Club after FDA laboratory analysis determined PrimeZEN Black 6000, a product promoted to improve sexual function for men, contains tadalafil and sildenafil.
Recalls & Warnings
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.
Recalls & Warnings
March 23, 2019
BLUEFUSION Capsules for Sexual Enhancement Recalled
On March 21, 2019, Ata Int. Inc. issued a recall of its BLUEFUSION capsules, which are promoted for sexual enhancement, because FDA analysis found them to contain sildenafil, tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin and daidzein.
Recalls & Warnings
April 25, 2013
FDA Warns Consumers of Sexual Enhancement Supplements Containing Drugs
On April 25, 2012, the FDA issued a warning to consumers, urging them not to purchase or use two sexual enhancement products which were found to contain undeclared drugs.
Recalls & Warnings
May 08, 2013
Three Sexual Enhancement Supplements Recalled for Undeclared Drug Risk
On May 7, 2013, BeaMonstar Products issued a voluntary recall of sexual enhancement supplements SexVoltz and Velextra because they were found to contain an undeclared drug.
Recalls & Warnings
March 21, 2013
FDA Warns Consumers: Three Sexual Enhancement Supplements Found To Contain Drugs
On March 21, 2013, the FDA warned consumers not to purchase or use three sexual enhancement dietary supplements, Rock-It Man, Libido Sexual Enhancer, and Stiff Days, because they were found to contain sildenafil or sildenafil analogues.
Recalls & Warnings
July 01, 2022
Male Enhancement Supplements Sold on Amazon Recalled
On January 27, 2022, Loud Muscle Science LLC issued a voluntary recall of various lots of Launch Sequence supplements because they were found to contain the prescription drug Tadalfil.
Recalls & Warnings
April 05, 2022
Sexual Enhancement Capsules for Men Recalled
On April 1, 2022, F&S Medical Supply, dba Pink Toyz, recalled one lot of Pink Pussycat 3000 mg capsules to the consumer level because FDA analysis found them to contain sildenafil.
Recalls & Warnings
December 19, 2013
Seller of Sexual Enhancement Supplement and Tea Drink Warned for Drug Ingredients and Drug Claims
On December 5, 2013, the FDA issued a warning letter to Green Planet, Inc. following a facility inspection which found the company's sexual enhancement supplement Night Bullet to contain the drugs sulfohydroxyhomosildenafil, thioaildenafil and aminotadalafil.
Recalls & Warnings
May 02, 2015
Three Sexual Enhancement Supplements Contain Prescription Drug
On April 30, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplements listed below because they were found to contain sildenafil. Each was identified during an examination of international mail shipments:
Recalls & Warnings
March 11, 2015
Three Male Enhancement Supplements Found to Contain Drug
On March 3, 2015, the FDA warned consumers not to buy or use the following three sexual enhancement supplements because they were found to contain an undeclared sildenafil (each was identified during an examination of international mail shipments):
Recalls & Warnings
March 06, 2015
Four Male Enhancement Supplements Found to Contain Drug
On March 5, 2015, the FDA warned consumers not to buy or use the following four sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
April 17, 2018
Sexual Enhancement Supplement Recalled
On April 16, 2018, Epic Products, LLC, recalled its sexual enhancement supplement Euphoric because it was found to contain undeclared sildenafil and tadalafil.
Recalls & Warnings
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.
Recalls & Warnings
March 26, 2019
LEOPARD Miracle Honey Recalled
On March 22, 2019, USA LESS issued a recall of all lots of LEOPARD Miracle Honey, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
December 19, 2020
FDA Finds Unapproved Drugs in Many Weight Loss and Sexual Enhancement Products Sold Online
On December 18, 2020, the FDA warned consumers that certain products promoted for weight loss, body building, sexual enhancement, pain relief, sleep, and other uses because may contain harmful ingredients.
Recalls & Warnings
August 20, 2024
Two Sexual Enhancement Supplements Sold on Amazon Recalled
On August 20, 2024, Veata LLC Endurance Pro Energy Boost capsules and Boulla LLC Boom Max capsules were recalled because they contain sildenafil, a prescription medication which is not permitted in dietary supplements.
Recalls & Warnings
November 30, 2023
Original The Rock Capsules Recalled Due to Undeclared Sildenafil
On October 18, 2023, Noah’s Wholesale, LLC issued a nationwide recall of one lot of the company’s Original The Rock capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.
Clinical Update
9/30/2015
Inaccurate Yohimbe Labels
Yohimbe supplements contain an active compound, yohimbine, which is an old drug for erectile dysfunction. A recent study found that most yohimbe supplements don't list the amount of yohimbine they contain, and those that do are typically inaccurate — similar to what ConsumerLab.com has found. For more about the study as well as our own tests of products, see the Sexual Enhancement Supplements Review >>
Recalls & Warnings
April 22, 2015
FDA Warns Consumers Not to Use Male Enhancement Supplement
On April 21, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Extreme Diamond 3000 because it was found to contain desmethyl carbodenafil and dapoxetine.
Recalls & Warnings
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):
Recalls & Warnings
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.
Recalls & Warnings
July 01, 2015
Undeclared Drugs Found In Male Enhancement Supplements
On June 10, 2015, the FDA issued a warning letter American Lifestyle, following tests which found the company's sexual enhancement supplements Vicerex and Sudibil-Xr to contain the undeclared drugs propoxyphenyl thioaildenafil and tadalafil.
Recalls & Warnings
May 03, 2013
Recall: Two Sexual Enhancement Supplements Containing Undeclared Drugs
On May 1, 2013, American Lifestyle issued a voluntary recall of all lots of sexual enhancement supplements Vicerex and Black Ant because they were found to contain undeclared prescription drugs.
Recalls & Warnings
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:
Recalls & Warnings
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):
Recalls & Warnings
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:
Recalls & Warnings
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 ...
Recalls & Warnings
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.
Recalls & Warnings
August 25, 2023
FDA Warns Consumers Not to Use Big Guys Male Energy Supplement
On August 22, 2023, the FDA warned consumers not to buy or use BIG GUYS Male Energy Supplement after FDA laboratory analysis found it to contain undeclared sildenafil.
Recalls & Warnings
September 06, 2023
WEFUN Capsules Recalled Due to Undeclared Sildenafil
On August 25, 2023, WEFUN Inc. issued a recall of 300 boxes of WEFUN Capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.
Recalls & Warnings
February 13, 2023
FDA Finds Prescription Drug in “100% Natural” Weight Loss Supplement
On February 8, 2023, the FDA warned consumers not to buy or use Alfia 100% Natural Weight Loss Capsules after FDA laboratory analysis confirmed the presence of sibutramine.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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:
Recalls & Warnings
April 04, 2013
Three More Sexual Enhancement Supplements Found To Contain Undeclared Drugs
On April 3, 2013, the FDA warned consumers that the sexual enhancement supplements AFFIRM XL, Love Rider and Ninja Mojo were found to contain undeclared erectile dysfunction drugs. Consumers are urged to stop using these supplements immediately.
Recalls & Warnings
April 10, 2013
Recall: Sexual Enhancement Supplement Containing Undeclared Drug
On April 1, 2013, Consumer Concepts, Inc. issued a voluntary nationwide recall of ROCK-It MAN Male Enhancement Capsules, a dietary supplement promoted for sexual enhancement which was found to contain undeclared hydroxythiohomosildenafil, an analogue of the prescription drug sildenafil.
Recalls & Warnings
August 15, 2015
FDA Warns Seller of Tainted Enhancement Supplements
On July 31, 2015, the FDA issued a warning letter to R Thomas Marketing following a review of the company's website, which found it sold the male enhancement supplements Black Ant, Herb Viagra, Real Skill and Stree Overlord . These supplements contain the undeclared sildenafil.
Recalls & Warnings
May 15, 2016
Sexual Enhancement Supplements Recalled
On May 10, 2016, SOS Telecom, Inc. issued a recall of the following sexual enhancement supplements, which were found to contain undeclared sildenafil:
Recalls & Warnings
August 01, 2017
"Man of Steel" Sexual Enhancement Supplements Recalled
On July 27, 2017, Man of Steel recalled its Man of Steel 1 and Man of Steel 2 sexual enhancement supplements because they were found to contain undeclared sildenafil.
Recalls & Warnings
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.
Recalls & Warnings
December 23, 2016
Twelve Sexual Enhancement Supplements Found to Contain Prescription Drug
On December 22, 2016, the FDA warned consumers not to buy or use the following twelve sexual enhancement supplements because they were found to contain undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
December 01, 2017
Nutra Labs Recalls Sexual Enhancement Supplements Containing Undeclared Drugs
On November 30, 2017, Nutra Labs Inc. recalled certain lots of its sexual enhancement supplements Bull 1800 mg Capsules and Chao Jimengnan 150 mg Tablets because they were found to contain undeclared sildenafil.
Recalls & Warnings
September 04, 2018
Federal Court Shuts Down Maker of Sexual Enhancement Products
On August 30, 2018, the FDA announced that U.S.
Recalls & Warnings
February 10, 2022
Three Sexual Enhancement Supplements Sold on Amazon Recalled
On February 8, 2022, specific lots of three male sexual enhancement supplements, Red Mammoth capsules, MAC DADDY RED capsules, MAC DADDY PURPLE capsules, and The Red Pill capsules, were recalled because Amazon laboratory analyses found them to contain undeclared ...
Recalls & Warnings
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
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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 :
Recalls & Warnings
June 22, 2023
FDA Warns Warrior Labz for Selling Products with Steroid-Like Substances and Prescription Drugs
On June 12, 2023, the FDA issued a warning letter to Warrior Labz SARMS following inspection of the company’s website and social media, which found that the company sold the following products labeled as containing steroid-like substances known as selective androgen receptor modulators ...
Recalls & Warnings
December 29, 2016
Sexual Enhancement Supplement Contains Prescription Drug
On December 22, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Power Male Sexual Stimulant because it was found to contain sildenafil. This supplement was identified during an examination of international mail shipments.
Recalls & Warnings
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.
Recalls & Warnings
April 10, 2021
Three More Male Enhancement Products Recalled Due to Undeclared Drugs
Between March 30 and April 5, 2021, three companies issued recalls of their male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.
Recalls & Warnings
April 02, 2021
Three Male Enhancement Products Recalled Due to Undeclared Drugs
Between March 24 and 26, 2021, three companies issued recalls of their male enhancement capsules because FDA analysis found them to contain sildenafil and tadalafil.
Recalls & Warnings
February 17, 2021
Adam’s Secret Male Enhancement Products Recalled Due to Undeclared Drugs
On February 15, 2021, adamssecret.co issued a recall of all lots of Adam's Secret Extra Strength 1500 and Adam's Secret Extra Strength 3000 male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.
Recalls & Warnings
May 19, 2018
Sexual Enhancement Supplements Containing Undeclared Drugs Recalled
On May 17, 2018, Shoreside Enterprises, Inc., recalled certain lots of its sexual enhancement supplements 7K and Poseidon 4500 (Extreme 1000 mg) because they were found to contain undeclared sildenafil and/or tadalafil.
Recalls & Warnings
December 19, 2017
Blue Pearl All Natural Enhancement Supplement Recalled
On December 13, 2017, Marmex Corp. recalled all lots of its sexual enhancement supplements Blue Pearl All Natural Male Enhancement Supplement, 500mg because they were found to contain undeclared sildenafil.
Recalls & Warnings
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.
Recalls & Warnings
March 13, 2015
Three Weight Loss Supplements Found to Contain Drugs
The FDA recently warned consumers not to buy or use the following weight loss supplements because they were found to contain undeclared drugs. Each was identified during an examination of international mail shipments.
Recalls & Warnings
February 07, 2024
Sustain and Schwinnng Male Enhancement Supplements Recalled
On February 2, 2024, Today the World issued a recall of all lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules after FDA analysis found the supplements to contain undeclared prescription drugs tadalafil and nortadalafil.
Recalls & Warnings
December 26, 2023
Total Body Nutrition, TBN Labs, and Loud Muscle Science Banned from Selling Adulterated and Misbranded Dietary Supplements
On December 11, 2023, Total Body Nutrition LLC, TBN Labs LLC, and Loud Muscle Science LLC, as well as the companies’ owner, Mohammed Islam, were prohibited by federal court from manufacturing and distributing adulterated and misbranded dietary supplements.
News Release
February 05, 2012
Fish oil and multivitamins most popular supplements in ConsumerLab.com survey -- Internet most popular place to shop
WHITE PLAINS, NEW YORK — FEBRUARY 5, 2012 — A survey of over 10,000 savvy consumers of supplements shows the most popular supplements to be fish oil, multivitamins, vitamin D, calcium and CoQ10, in that order.
Product Review
Maca Supplements Review
Choose the Best Maca Supplement. Make Sure Your Maca Supplement Isn't Contaminated With Lead.
Product Review
DHEA Supplements Review
Choose the Best DHEA Supplement. Beware of Big Differences in Dose and Price.
Recalls & Warnings
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.
Product Review
Breast Enhancement Supplements Review Article
Do Breast Enhancement Supplements Really Work? See the Evidence For and Against Breast Enhancement Supplements.
News Release
August 31, 2011
ConsumerLab.com analyzes supplements for sexual dysfunction -- Only three out of ten products selected for testing pass
WHITE PLAINS, NEW YORK — August 31, 2011 — Only three out of ten supplements selected for testing that are for sexual enhancement passed ConsumerLab.com's latest investigation.
Recalls & Warnings
June 22, 2017
FDA Finds Hidden Drug Ingredients in Sexual Enhancement Supplements
On June 22, 2017, the FDA warned consumers that the following sexual enhancement supplements were found to contain undeclared sildenafil, tadalafil and/or dapoxetine. Use the links below to read the complete warning letter for each:
- Triple Premium Zen Gold 1300 mg
Recalls & Warnings
March 21, 2017
Twenty-one Sexual Enhancement Products Recalled
On March 7, 2017, A&H Focal Inc. issued a recall of the following sexual enhancement supplements because they were found to contain drugs such as sildenafil, tadalafil, vardenafil:
Recalls & Warnings
March 04, 2017
Sexual Enhancement Supplements Found to Contain Drugs
On March 3, 2017, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared drugs:
Recalls & Warnings
February 04, 2017
FDA Warns Four Sexual Enhancement Supplements Contain Prescription Drug
The FDA recently warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared sildenafil.
Recalls & Warnings
November 11, 2016
Male Enhancement Supplement Contains Hidden Drug
On November 9, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Ready Man! because it was found to contain sildenafil and phenolphthalein.
Recalls & Warnings
March 20, 2016
Salute Capsules Contain Hidden Drugs
On March 17, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Salute Capsules because it was found to contain sildenafil, thiosildenafil, and sulfoaildenafil.
Recalls & Warnings
March 04, 2016
FDA Warns Consumers Not To Use Sexual Enhancement Supplement
On March 3, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Sextra because it was found to contain sildenafil.
Recalls & Warnings
February 27, 2016
Enhancement Supplement Contains Undeclared Drug
The FDA recently warned consumers not to buy or use the sexual enhancement supplement Neophase Natural Sex Enhancer because it was found to contain hydroxyacetildenafil.
Recalls & Warnings
January 28, 2013
Recall: Male Sexual Enhancement Supplement Found to Contain Prescription Drug
On January 24, 2013, D&S Herbals, LLC, dba Freedom Trading, announced a voluntary recall of one lot of the male sexual enhancement dietary supplement Super Power because it was found to contain undeclared sildenafil.
Recalls & Warnings
May 19, 2020
FTC Sends Refund Checks to Consumers of Unproven Weight Loss and Sexual Enhancement Supplements
On May 19, 2020, the FTC announced it is mailing 143,636 checks totaling more than $8,500,000 to consumers who purchased deceptively marketed supplements.
Recalls & Warnings
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:
Recalls & Warnings
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.
Recalls & Warnings
March 13, 2013
Recall: Male Sexual Enhancement Supplement Containing Drugs
On March 12, 2013, Green Planet, Inc. issued a recall of one lot of the male sexual performance enhancer supplement Night Bullet because it was found to contain trace amounts of sulfohydroxyhomosildenafil and aminotadalafil, analogues of the prescription drug sildenafil.
Recalls & Warnings
December 14, 2010
FDA Warns Consumers to Avoid Man Up Now Capsules
On December 14, 2010, the U.S. FDA warned consumers not to use Man Up Now capsules, marketed as a dietary supplement for sexual enhancement, because they contain a variation of an active drug ingredient found in Viagra that can dangerously lower blood pressure.
Recalls & Warnings
May 10, 2013
Seller Of Sexual Enhancement and Hormonal Balance Supplements Warned For Manufacturing Violations
On April 26, 2013, the FDA issued a warning letter to Pristine Bay, L.L.C.
Recalls & Warnings
October 22, 2014
Supplements Recalled Years Ago Remain on the Market, Still Contain Hidden Drugs
On October 21, 2014, a report in the Journal of the American Medical Association (JAMA) revealed that almost 10% of the supplements that have been recalled over the past few years are still on the market - and many still contain the hidden drugs which prompted their initial recall.
Recalls & Warnings
November 16, 2019
Silver Bullet Supplement for Men Recalled
On November 13, 2019, Nature's Rx issued a recall of one lot of Silver Bullet male enhancement capsules because FDA analysis found it to contain sildenafil.
Recalls & Warnings
April 17, 2021
NS NY Distributor Inc Male Enhancement Products Recalled Due to Undeclared Drugs
On April 8, 2021, NS NY Distributor Inc issued a recall of all lots of Premium Orgazen 7000 and Ginseng Power 5000 male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.
Recalls & Warnings
July 15, 2024
Hard Steel Supplements for Men Recalled
On July 12, 2024, Supercore Products Group issued a recall of Hard Steel Capsules and Gold Hard Steel Liquid which are used for male erectile dysfunction. The FDA analysis found the capsules to contain sildenafil and acetaminophen.
Recalls & Warnings
March 29, 2013
Prescription Drugs Found In Prostate and Sexual Enhancement Supplements
October 24, 2012 the FDA issued a warning letter to USA Far Ocean Group Inc./ Health & Beauty Group Inc. because a number of the company's dietary supplements were found to contain pharmaceutical drugs, or were promoted with statements that constitute drug claims.
CL Answer
Is Relief Factor likely to relieve aches and pains, and is it safe?
Find out if the dietary supplement Relief Factor is likely to help relieve aches and pains, if it is safe, and if it is worth the cost.
Recalls & Warnings
November 06, 2009
FDA Warns that "Stiff Nights" Enhancement Supplement Contains Undeclared Drug
On November 5, 2009 the U.S. Food and Drug Administration (FDA) warned consumers that Stiff Nights, a product marketed as a dietary supplement for sexual enhancement, contains an ingredient that can dangerously lower blood pressure and is illegal.
Recalls & Warnings
December 12, 2015
Sexual Enhancement Supplement Recalled
On December 11, 2015, Reesna Inc. issued a recall of its sexual enhancement supplements Fuel Up Plus and Fuel Up High Octane which were distributed in August 2015 and were found to contain undeclared hydroxythiohomosildenafil.
Recalls & Warnings
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.
Recalls & Warnings
January 12, 2016
Twenty-four Male Enhancement Supplements Recalled
On January 9, 2016, R Thomas Marketing LLC. in conjuction with Just Enhance LLC, issued a recall of the following sexual enhancement supplements because they were found to contain sildenafil:
Recalls & Warnings
May 29, 2018
FDA Warns Seller of "Aromatase Inhibitor" Supplement
On May 18, 2018, the FDA issued a warning letter to Performance Nutrition Formulators LLC d.b.a. VMI Sports because its product Arimistane contains Androsta-3,5-Diene-7,17-Dione, an ingredient that the FDA considers to be a new drug and not a dietary supplement ingredient.
CL Answer
Have any supplements been shown to increase women's libido?
Learn more about supplements that may increase women's libido, including DHEA and maca.
Recalls & Warnings
December 21, 2019
Men's Enhancement Supplement Recalled
On December 17, 2019, Motto International Corp all lots of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000, to the consumer leve because FDA analysis has found they contain tadalafil.
Recalls & Warnings
September 03, 2020
Red-E Male Enhancement Capsule Recalled
On September 1, 2020, The Protein Shoppe, LLC issued a recall of Red-E male enhancement capsules because FDA analysis found it to contain sildenafil.
Recalls & Warnings
January 03, 2024
FDA Warns Amazon for Selling Men’s Supplements Containing Prescription Drugs
On December 20, 2023, the FDA issued a Warning Letter to Amazon.com, Inc.
Recalls & Warnings
December 14, 2023
Pain Relief Tea Recalled, Found to Contain Prescription Drugs
On December 13, 2023, WS Global issued a recall of all lots of the company’s Himalayan Pain Relief Tea after products were found to contain diclofenac and dexamethasone, prescription drugs that are not listed on the product’s label.
Recalls & Warnings
May 17, 2012
FDA Warns of Drug Ingredients in Three Sexual Enhancement Supplements
On May 16, 2012, the U.S. FDA advised consumers not to purchase or use the following three sexual enhancement products: Boost - Ultra Sexual Enhancement Formula (sold on www.boostultra.biz), Firminite (sold on www.firminite.com), and VMaxx Rx (sold on www.vmaxxrx.com).
Recalls & Warnings
April 03, 2012
"France T253" Enhancement Supplement Contains Hidden Drug
April 3, 2012: The U.S. Food and Drug Administration (FDA) is advising consumers not to purchase or use “France T253,” a product for sexual enhancement. This product is promoted and sold on various Web sites, such as ebay.com.
Recalls & Warnings
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).
CL Answer
Which supplements can help to lower blood pressure?
Supplements to lower blood pressure, including CoQ10, vitamin C, fish oil, and olive oil, are all explored to find out what works.
Recalls & Warnings
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.
Recalls & Warnings
May 15, 2008
Feds Seek Millions from Seller of Enzyte Sexual Enhancement Supplement
According to an article in the Cincinnati Enquirer, on Wednesday, May 14, federal prosecutors told a U.S. District Court judge that the government could seek as much as $450 million in forfeitures from the sellers of Enzyte, a male sexual enhancement supplement.
Recalls & Warnings
October 13, 2018
Pharmaceutical Drugs Found In Dietary Supplements Pose Danger to Consumers
Almost 800 dietary supplements sold between 2007 and 2016 contained unapproved pharmaceutical ingredients, according to a study published today in the Journal of the American Medical Association (JAMA).
CL Answer
Which supplements, foods or diet and lifestyle changes help relieve acid reflux (heartburn), and which worsen it?
Find out which supplements and foods can help relieve acid reflux, and which can make it worse.
CL Answer
When taking a statin drug like Lipitor or Crestor, are there supplements I should avoid or take?
Learn about the interactions between certain supplements and atorvastatin (Lipitor), rosuvastatin (Crestor), and other cholesterol-lowering statins.
Recalls & Warnings
June 30, 2022
FDA Warns Seller of Vision and Allergy Supplements
On May 26, 2022, the FDA issued a warning letter to Golden Lab LLC following an inspection of the website, which found statements about the company’s DoctoRx’s Optimal Formula Ocular Pressure & Optic Nerve Support Formula Ocular Health Capsule, DoctoRx’s Optimal Formula ...
News Release
July 21, 2010
Tests of "muscle enhancement" supplements show quality problems with some creatine and branched-chain amino acid products -- Review of Muscle Enhancement Supplements published by ConsumerLab.com
WHITE PLAINS, NEW YORK — July 21, 2010 — Athletes often turn to supplements to enhance muscle strength and recovery. New tests of such supplements by ConsumerLab.
Recalls & Warnings
November 21, 2010
FDA Warns Consumers Not to Use Vigor-25
On November 19, 2010, the U.S.
Recalls & Warnings
September 18, 2012
Men’s Sexual Enhancement Supplement Containing Prescription Drug Recalled
On September 12, 2012, Body Basics Inc. issued a voluntary nationwide recall of ACTRA-Sx 500 Dietary Supplement Capsules after independent laboratory testing confirmed the supplement contains the prescription drug sildenafil citrate.
Recalls & Warnings
May 17, 2013
Hoodia, Sexual Enhancement Supplements and More Found To Be Adulterated, Misbranded
On March 01, 2013, the FDA issued a warning letter to Desert Rose Manufacturing, Inc.
Recalls & Warnings
October 14, 2015
Recall of Male Enhancement Supplement Expanded
On October 9, 2015, TF Supplements expanded its previous recall of two lots of RHINO 7 sexual enhancement supplements, which were found to contain the undeclared drugs desmethyl carbondenafil and dapoxetine, to include all lots.
Recalls & Warnings
September 26, 2015
Male Enhancement Supplement Containing Antidepressant Recalled
On September 25, 2015, TF Supplements issued a recall of two lots of the sexual enhancement supplement RHINO 7, which were found to contain the undeclared drugs desmethyl carbondenafil and dapoxetine.
Recalls & Warnings
February 19, 2014
Seller of Sexual Enhancement Supplements Warned For Manufacturing Violations
On February 11, 2014, the FDA issued a warning letter to Maximus Niterider International Group, Inc.
Recalls & Warnings
December 03, 2016
Male Enhancement Supplement Recalled
On November 29, 2016, MS Bionic, Inc. issued a recall of all lots of Megajex Natural Male Sex Enhancer capsules because they were found to contain tadalafil and sildenafil.
Recalls & Warnings
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.
News Release
November 18, 2008
Adulteration Suspected with Some "Memory" Supplements -- Few Ginkgo and Huperzine Supplements Pass ConsumerLab.com Tests; Quality High for Acetyl-L-Carnitine
WHITE PLAINS, NEW YORK — NOVEMBER 18, 2008 — Tests by ConsumerLab.com of Ginkgo biloba supplements show that few products meet quality standards.
News Release
November 13, 2006
Tests of "muscle" supplements finds some "weak" products but most contain expected creatine, HMB, or amino acids — Review of muscular enhancement supplements published by ConsumerLab.com
WESTCHESTER, NEW YORK — MONDAY, NOVEMBER 13, 2006 — Bodybuilders and athletes often turn to supplements to enhance muscle size and strength.
News Release
September 19, 2006
DHEA supplements, touted for anti-aging and strength, reviewed by ConsumerLab.com — Testing finds one brand with 215% of the labeled amount
WHITE PLAINS, NEW YORK — SEPTEMBER 19, 2006 — New tests of supplements containing the hormone DHEA found most to contain their claimed amounts of the controversial ingredient, but one provided 215% of its stated amount, the testing company ConsumerLab.com reported today.
Recalls & Warnings
July 20, 2021
Alpha Male Plus Recalled
On July 16, 2021, Alpha Male Plus issued a recall of Alpha Male Plus Male Enhancer fruit chews because FDA analysis found them to be contaminated with tadalafil.
News Release
January 25, 2006
Sexual enhancement supplements analyzed by Consumerlab.com
WESTCHESTER COUNTY, NEW YORK — JANUARY 25, 2006 — ConsumerLab.com announced today that it found only six out of eleven supplements used for sexual enhancement to contain key ingredients listed on their labels and meet other quality criteria.
Recalls & Warnings
June 02, 2020
FTC Sends Refund Checks for "ReJuvination" Supplement
On June 1, 2020, the FTC announced it is mailing 1,310 checks totaling nearly $149,000 to consumers who purchased ReJuvination, a product deceptively marketed as a cure-all for various age-related conditions, including cell damage, heart attack damage, brain damage, and deafness.
Recalls & Warnings
May 30, 2020
FTC Sends Refund Checks for TrueAloe and AloeCran
On May 26, 2020, the FTC announced it is mailing 22,581 checks totaling more than $470,000 to consumers who purchased deceptively marketed supplements, TrueAloe and AloeCran.
Recalls & Warnings
June 23, 2020
FTC Sends Refund Checks to Consumers of Deceptive "Free Trial" Scheme
On June 22, 2020, the FTC announced it is mailing 187,425 checks totaling more than $8.
Recalls & Warnings
November 20, 2020
FTC Files Complaint Against Two Supplement Companies for Deceptive Marketing
On November 20, 2020, the FTC approved a Part 3 administrative complaint against Health Research Laboratories, LLC, its owner Kramer Duhon, and Whole Body Supplements, LLC for making unverified claims that their products can prevent or treat diseases.
CL Answer
What is BPC-157, what is it used for and is it safe?
Find out about BPC-157, including what it's promoted for and if it is safe.
Recalls & Warnings
August 07, 2015
Male Enhancement and Weight Loss Supplement Containing Drugs Recalled
On August 6, 2015 Blue Square Market Inc. issued a recall of the following supplements which were found to contain undeclared drugs:
Recalls & Warnings
August 28, 2013
Maker of Sexual Enhancement Supplement Warned for Manufacturing Violations
On July 11, 2013, the FDA issued a warning letter to Precise Nutrition International Inc.
Recalls & Warnings
March 17, 2020
"Active Male" Supplement Recalled
On March 16, 2020, Natural Remedy Store recalled all lots of Active Male, 500mg, to the consumer level because FDA analysis has found the product contains tadalafil.
News Release
January 03, 2006
Tests of memory enhancing supplements by ConsumerLab.com reveals lead in some ginkgo
WESTCHESTER COUNTY, NEW YORK — TUESDAY, JANUARY 3, 2006 — In its new test report on Memory Enhancement Supplements, ConsumerLab.com has revealed finding significant amounts of lead in certain products on the market.
News Release
August 16, 2005
ConsumerLab.com tests potassium supplements — Report now online for sixteen products
WHITE PLAINS, NY — August 16, 2005 — ConsumerLab.com has released a new report on the quality of potassium supplements. Potassium is used to treat or prevent potassium deficiency caused by diuretic drugs ("water pills"), prolonged vomiting, diarrhea or laxative abuse.
News Release
September 24, 2003
Consumerlab.com finds new forms of creatine prone to problems — Test results of muscular enhancement supplements published online today
WHITE PLAINS, NY — September 24, 2003 — Testing by ConsumerLab.com of creatine supplements found problems with the majority of products sold in liquid, effervescent and chewable forms. Problems were not found among standard creatine "powder" products.
Recalls & Warnings
February 18, 2020
Seller of CoQ10, Resveratrol and More Warned for Manufacturing Violations
On February 5, 2020, the FDA issued a warning letter to R-Garden LLC, which found the company's Vitamin O, Gamma-Zyme, L.
Recalls & Warnings
December 27, 2019
Federal Court Shuts Down Three Supplement Companies With Serious Manufacturing Violations
Update: (1/23/20) ABH has issued a recall of all its products, which are sold under various brand names by over 800 distributors and retailers. More details are available in CL's post about this recall.
Recalls & Warnings
October 12, 2020
NutraClick to Pay $1.04 Million for Illegally Billing Consumers
On September 22, 2020, the Federal Trade Commission (FTC) announced that NutraClick LLC agreed to pay $1.04 million to settle FTC charges that the company was deceptively selling and billing consumers for supplements and beauty products.
Recalls & Warnings
June 16, 2020
Seller of Silver, Arginine, and More Warned for Manufacturing Violations
On June 1, 2020, the FDA issued a warning letter to Morningstar Minerals LLC, which found the company's products, including Silver Boost, to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...
Recalls & Warnings
May 23, 2013
Seller of Sexual Enhancement, Cholesterol, Resveratrol Supplements and More Warned For Drug Claims
On May 2, 2013, the FDA issued a warning letter to Alternative Health Supplements, following a review of the company's website, which found statements made about several dietary supplements, including Regenerect, Alligin, Astaxanthin Advantage, HDL Cholesterol Management, Resveratrol, Coral Calcium ...
News Release
April 21, 2003
Low quality ingredient appears widespread among Ginkgo supplements according to ConsumerLab.com; points to challenge for FDA's proposed regulations — Review of memory enhancement supplements released today
WHITE PLAINS, NY — April 21, 2003 — In contrast to its findings three years ago, ConsumerLab.com announced today that only 22% of the Ginkgo biloba supplements it recently tested met its quality standards. In late 1999, 75% of the products it tested met these standards.
News Release
September 24, 2002
Problems found with most sexual enhancement supplements evaluated by ConsumerLab.com — Only 9 of 22 products pass independent review
WHITE PLAINS, NY — September 24, 2002 — ConsumerLab.com announced today that nearly 60% of products failed to pass its independent Product Review of Sexual Enhancement Supplements. Sexual dysfunction is estimated to affect 43% of women and 31% of men in the U.S.
Recalls & Warnings
July 26, 2012
Sexual Enhancement Supplements Containing Prescription Drug Recalled
On July 20, 2012, CRM Laboratories issued a voluntary recall of all X-Rock 3 Day Pill For Men and Z-Rock All Natural Male Supplements after FDA testing found these products contain the drugs sildenafil and hydroxythiohomosildenafil.
Recalls & Warnings
March 08, 2012
Rx Drugs Found in Weight Loss and Enhancement Supplements
On February 6, 2012, FDA issued a letter to Globe All Wellness, LLC warning that two of their products contain undeclared prescription drugs.
Recalls & Warnings
December 19, 2012
Sexual Enhancement Supplements Recalled Due To Undeclared Drugs
On December 17, 2012, Performance Plus Marketing, Inc.
Recalls & Warnings
September 21, 2012
Sexual Enhancement Supplements For Men and Women Recalled Due to Prescription Drug Risk
On August 23, 2012, Evol Nutrition Associates Inc./Red Dawn issued a voluntary recall of Mojo Nights after FDA testing revealed the male sexual enhancement supplement contains undeclared prescription drugs tadalafil and sildenafil.
Recalls & Warnings
December 17, 2010
FDA Steps Up Efforts to Battle Tainted Supplements
On Dec. 15, 2010, the Food and Drug Administration (FDA) took new steps aimed at keeping consumers safe from harmful products that are marketed as dietary supplements and that contain undeclared or deceptively labeled ingredients.
Recalls & Warnings
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.
Recalls & Warnings
September 16, 2015
Weight And Enhancement Supplement Recall Expanded
On September 11, 2015, One Minute Miracle Inc. issued a recall of all lots the following supplements which were found to contain undeclared drugs:
Recalls & Warnings
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 ...
Recalls & Warnings
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, ...
Recalls & Warnings
February 03, 2016
Seller of Weight and Enhancement Supplements Warned For Drug Claims
On December 11, 2015, the FDA issued a warning letter to The One Minute Miracle, Inc., following a review of the company's website which found statements made about Miracle Diet 30 and Miracle Rock 48 to be drug claims.
Recalls & Warnings
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.
Recalls & Warnings
April 09, 2003
Recall of Dangerous Sexual Enhancement Supplement Illegally Containing Viagra Ingredient
On April 4, 2003, the U.S. Food and Drug Administration's MedWatch program announced that Ultra Health Laboratories, Inc. and Bionate International, Inc. are warning consumers not to purchase or consume a product known as Vinarol tablets.
Recalls & Warnings
December 14, 2009
Nationwide Recall of Sexual Enhancement Supplements Containing Drug-like Compound
On December 14, 2009, the Federal Drug Administration (FDA) posted a notice on its website regarding the recall of many sexual enhancement supplements sold by Atlas Operations, Inc.
Recalls & Warnings
December 01, 2018
Seller of 5-HTP, Potassium & More Warned for Manufacturing Violations
On September 7, 2018, the FDA issued a warning letter to The Delano Company, Inc.
Recalls & Warnings
September 03, 2019
Federal Court Shuts Down Two Supplement Companies Selling Weight, Joint Health and Other Supplements
On September 3, 2019, a U.S. District Court entered a consent decree of permanent injunction against Basic Reset and Biogenyx, two Tennessee-based companies that sell dietary supplements and other product promoted for health benefits.
Recalls & Warnings
May 25, 2019
Department of Justice Files Complaint to Shut Down Supplement Company
On May 23, 2019, the United States Department of Justice announced a complaint seeking a permanent injunction has been filed against dietary supplement marketers Helen Chian and Jim Chao, president and company manager of Confidence USA Inc.
Clinical Update
11/09/2021
Saw Palmetto Concern
Does saw palmetto cause sexual dysfunction? Get the details in the updated Concerns and Cautions section of our Prostate Supplements Review.
Clinical Update
11/24/2015
Herbal Arousal
We have previously reported that ashwagandha extract may improve fertility in men. A new study suggests that it can improve sexual function in women. Details about the product and dosage, and our tests of products on the market, are found in the Ashwagandha Review >>
Clinical Update
12/05/2023
Caution With Supplements for Libido
Be aware that supplements sold in the U.S. to improve sexual function may contain undeclared medications, especially those packaged a particular way. Learn more in the Concerns and Cautions section of our review.
Clinical Update
5/21/2024
Arginine for Libido, Mood?
Did taking L-arginine improve sexual function or mood in women with depression? Find out what a recent study showed in the What It Does section of our L-Arginine Supplements Review, which includes our Top Picks.
Clinical Update
7/25/2024
Statin Interaction With Herb
An herb often promoted for libido may negatively interact with some statins and other medications. Get the details in the Concerns and Cautions section of our Sexual Enhancer Supplements Review.
Clinical Update
3/19/2024
Vitamin D for ED?
Did taking vitamin D improve sexual function among older men? Find out what a recent study showed in our Vitamin D Supplements Review. Also see our Top Picks for vitamin D.
Recalls & Warnings
August 30, 2015
Weight and Enhancement Supplements Recalled
On August 27, 2015, One Minute Miracle Inc. issued a recall of one lot each the following supplements which were found to contain undeclared drugs:
Recalls & Warnings
June 23, 2017
FDA Warns Seller of Menopause, Sexual Enhancement, Prostate Supplements and More For Manufacturing Violations
On May 26, 2017 the FDA issued a warning letter to Star Health & Beauty LLC, following a facility inspection which found the company's products, including Nu Essentials Royal Jelly Capsules, NuMan Male Enhancement Capsules, Star's Male Potency Tonic, NuGen HP, She Max HP, and V Max ...
Recalls & Warnings
April 18, 2012
X-Rock Contains Undeclared Drug Ingredient
April 18, 2012: The Food and Drug Administration (FDA) is advising consumers not to purchase or use “X-Rock,” a product for sexual enhancement manufactured by CRM Laboratories and sold on various websites, including www.xrockme.com.
Recalls & Warnings
December 30, 2007
FDA Warns Consumers Not to Use Several "Shangai" Sexual Enhancement Supplements
On December 28, 2007, the U.S. Food and Drug Administration (FDA) advised consumers not to buy or use Super Shangai, Strong Testis, Shangai Ultra, Shangai Ultra X, Lady Shangai, and Shangai Regular, also marketed as Shangai Chaojimengnan, products.
Clinical Update
9/17/2019
Omega-3s for Cognition?
Several studies have attempted to boost cognition and memory in healthy people using omega-3 supplements from fish or krill oil. Find out if they succeeded, including a recent study among adolescents, in the Memory Enhancement in Healthy Individuals section of the Fish Oil Supplements Review. Also see our Top Picks among products.
Clinical Update
10/08/2019
Fish Oil to Improve Cognition?
See the results of the most recent study of fish oil to improve memory and cognition in the Memory Enhancement section of the Fish Oil Supplements Review. Also see our Top Picks for fish oil.
Clinical Update
2/04/2020
Problems With Huperzine A
A recent analysis of supplements claiming to contain huperzine A (promoted for memory enhancement) found problems with most products. For details see the Concerns and Cautions section of the Huperzine A Supplements Review. Also learn what clinical studies have shown with huperzine A in the What It Does section and see which huperzine A supplements have been Approved by CL.
Clinical Update
8/28/2020
Concern Over Memory Supplement Quality
Many supplements with phosphatidylserine – promoted for memory enhancement -- do not contain their listed amounts of this ingredient, according to a new report. Get details and learn what clinical studies show with phosphatidylserine in our updated answer to the question: Do either phosphatidylserine or phosphatidylcholine help with memory and cognition?
Clinical Update
3/05/2024
Fish Oil for Memory?
Did taking fish oil improve cognitive function or memory among older people with depression in a recent study? Find out in the Memory Enhancement section of our Fish Oil Supplements Review, which includes our Top Picks for fish oil.
Also see: Do any supplements, foods or lifestyle modifications help with brain function, like memory and cognition?
Clinical Update
11/17/2023
Calanus Oil for Memory?
Does supplementing with calanus oil, a source of omega-3 fatty acids, improve memory in older men and women? Find out what research suggests in the Memory Enhancement in Healthy Individuals section of our Fish Oil Supplements Review.
Also see: Do any supplements, foods or lifestyle modifications help with brain function, like memory and cognition?
Clinical Update
3/22/2022
Fish Oil: Cognitive Benefit in Healthy People?
Does fish oil supplementation improve cognition in healthy people? See what a recent study showed in the Memory Enhancement in Healthy Individuals section of our Omega-3 Fatty Acid Supplements Review.
Also see our answer to the question: Do any supplements or foods help with brain function, like memory and cognition?
Recalls & Warnings
January 29, 2018
Seller of Male Enhancement, Prostate Supplements & More Warned for Drug Claims
On January 10, 2018, the FDA issues a warning letter to USA Labs AKA Power Source Distributors, Inc following a review of the company's website which found statements made about its products, including Maximum Male, Beta 300 (Beta Prosturol), Chromium Max 1000, DHEA, Healthy Cold-X and ...
Recalls & Warnings
February 17, 2018
FDA Warns Seller Reishi Mushroom Supplements
On February 7, 2018, the FDA issued a warning letter to Reishi D. International, Inc., following a facility inspection which found the company's Reishi D.
Recalls & Warnings
November 22, 2017
FDA Warns Distributor of "Testosterone Wellness for Men"
On November 8, 2017, the FDA sent a warning letter to Vita-Pure, Inc.
Recalls & Warnings
June 20, 2017
Beware of Bodybuilding Supplements, FDA Warns
On June 20, 2017, the FDA warned consumers to beware of bodybuilding products because a number of these products have been found to contain steroids or steroid-like substances. Such products could cause serious and even life-threatening health risks, including:
Recalls & Warnings
July 12, 2017
More Bodybuilding Supplements Recalled
On July 11, 2017, Andropharm recalled two bodybuilding supplements, Sten Z and M1 Alpha, because these products contain derivatives of anabolic steroids.
Recalls & Warnings
July 13, 2006
FDA Warns About Sexual Enhancement Supplements with Dangerous Ingredients
On July 12, 2006, the Federal Drug Administration (FDA) warned consumers not to purchase or consume Zimaxx, Libidus, Neophase, Nasutra, Vigor-25, Actra-Rx, or 4EVERON.
Recalls & Warnings
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.
Recalls & Warnings
July 20, 2010
Recall of ED Supplement Containing Drug
On July 20, 2010, the U.S. FDA posted a news announcement from Good Health, Inc. regarding the recall of Vialipro, a sexual enhancement supplement sold nationally.
Recalls & Warnings
October 08, 2010
"Red Flags" for Spotting Tainted Supplements
In recent years, the FDA has identified hundereds of products marketed as dietary supplements or conventional foods with hidden drugs and chemicals. In reaction to this, the FDA recently created a flyer to help retailers spot questionable products. ConsumerLab.
Recalls & Warnings
October 25, 2016
Seller of Liquid Aloe & Mineral Supplement Warned for Manufacturing Violations
On August 10, 2016, the FDA issued a warning letter to Perfect Source Natural Products Inc.
Recalls & Warnings
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.
Recalls & Warnings
April 03, 2014
Maker of Green Coffee Bean Extract and Weight Loss Supplement Warned for Manufacturing Violations
On March 13, 2014, the FDA issued a warning letter to Libi Labs, Inc.
Recalls & Warnings
December 19, 2013
Maker of Joint Health Supplements Warned for Manufacturing Violations
On December 4, 2013, the FDA issued a warning letter to PurQuality, LLC.
Recalls & Warnings
October 25, 2013
Supplement Company Warned For Numerous Manufacturing Violations
On August 2, 2013, the FDA issued a warning letter to DNE Nutraceuticals, Inc., following a facility inspection which found the company's products to be adulterated because they were packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.
Recalls & Warnings
August 05, 2016
Seller of Fertilix Warned By FDA
On July 22, 2016, the FDA issued a warning letter to CellOxess LLC, following a review of the company's websites, social media pages and marketing literature which found statements made about Fertilix Preconceptual, Fertilix Low Dose and Fertilix Max to be drug claims.
Recalls & Warnings
July 23, 2016
Seller of GlucoCor Warned for Drug Claims
On June 30, 2016, the FDA issued a warning letter to MC-COR, LLC, following a review of the company's website and Facebook page which found statements made about its GlucoCor capsules to be drug claims.
Recalls & Warnings
March 08, 2016
Maker of Calcium and Vitamin C Supplements Warned for Manufacturing Violations
On September 17, 2015, the FDA issued a warning letter to Raphah, Inc.
Recalls & Warnings
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.
Recalls & Warnings
April 03, 2015
Health Canada Suspends Sales of Male Fern Products
On April 2, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced it has suspended the licenses of the natural health products containing the ingredient male fern (Dryopteris filix-max), due to concern over the safety of the ingredient when taken at higher doses.
Recalls & Warnings
February 16, 2012
Recall of Enhancement Supplement for Women -- Contains Drug
On Feb, 10, 2012, Regeneca, Inc. announced a voluntary nationwide recall of RegenArouse Natural Female Intimacy Enhancement. The product was distributed throughout the U.S. and Puerto Rico to Internet consumers. The product is distributed as a pink capsule sold individually in foil packets.
Recalls & Warnings
March 02, 2012
Recall of Enhancement Supplement for Men -- Contains Drug
On Feb, 24, 2012, Regeneca, Inc. announced a voluntary nationwide recall of all lots of RegenErect. The product was distributed throughout the U.S. and Puerto Rico to Internet consumers. The product is distributed as a blue capsule sold individually in foil packets with a UPC code of 816860010055.
Recalls & Warnings
April 18, 2013
Cardio, Energy and Sexual Enhancement Supplement Distributor Warned For Manufacturing Violations and Drug Claims
On December 21, 2012, the FDA issued a warning letter to ForMor Inc, dba ForMor International, following a facility inspection which found the company's Cardio Cocktail and Argenix dietary supplements to be adulterated because because they were prepared, packed, or held under conditions that do ...
Recalls & Warnings
September 13, 2010
ExtenZe Enhancement Supplements Seized in Canada
On August 19, 2010, Health Canada (Canada's health ministry) seized the sexual enhancement supplements "Male Enhancement ExtenZe" and "Women ExtenZe" which were imported from the U.S. Although legal and widely sold in the U.S.
Recalls & Warnings
June 27, 2012
Maker of Pain Relief, Virility, and Idebenone Products Warned of Violations by FDA
On June 19, 2012, the U.S. FDA warned ABCO Laboratories of Fairfield, Caliornia, a contract manufacturer, of violations of FDA regulations for its products IBU-RELIEF 12, Sexual Virility Max, and Idebenone Capsules.
Recalls & Warnings
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.
Recalls & Warnings
November 20, 2013
$2 Million In Weight Loss and "Fat-Burning" Supplements Seized
On November 12, 2013, U.S. Marshals seized more than $2 million worth of supplements from Georgia-based Hi-Tech Pharmaceuticals, Inc.
Recalls & Warnings
September 27, 2013
Company Warned For Distributing Weight Loss Supplement Containing DMAA, Drug Claims
On September 6, 2013, the FDA issued a warning letter to Pure Energy Products, Inc., following a facility inspection which found that the company distributes a weight loss supplement, called obestrim, which contains dimethylamylamine, or DMAA.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
November 03, 2004
FDA Warns of Sexual Enhancement Supplements Containing Prescription Drug
On November 2, 2004, the Food and Drug Administration (FDA)warned consumers not to purchase or to consume Actra-Rx or Yilishen, two products promoted and offered for sale on Web sites as "dietary supplements" for treating erectile dysfunction and enhancing sexual performance for men.
Recalls & Warnings
March 20, 2007
Recall of Adulterated Sexual Enhancement Supplement
As posted on the FDA website, on March 15, 2007, the company Barodon SF of Los Angeles, CA announced that it is conducting a voluntary nationwide recall of the company's supplement product sold under the name V.MAX.
Recalls & Warnings
May 29, 2003
Recall and Warning for Another Sexual Enhancement Supplement Illegally Containing Viagra Ingredient
On May 23, Best Life International, in cooperation with the U.S. Food and Drug Administration, warned consumers not to purchase or consume the product known as Viga.
Recalls & Warnings
November 20, 2013
Weight Loss Supplement Found to Contain Drugs
On November 19, 2013, the FDA warned consumers not to buy or use weight loss supplement Slim Max because it was found to contain sibutramine and phenolphthalein.
Recalls & Warnings
November 12, 2013
Weight Loss Supplement Found To Contain Drugs
On November 8, 2013, Health Canada warned consumers of a number of weight loss products that have been found to contain sibutramine or phenolphthalein, including Paiyouji Natural Slimming Capsules, which may be available for purchase to U.S. consumers through online retailers.
Recalls & Warnings
November 07, 2013
FDA Warns Consumers of Weight Loss Supplement Containing Multiple Drugs
On November 7, 2013, the FDA warned consumers not to buy or use Jimpness Beauty Fat Loss Capsules because they were found to contain sibutramine, phenolphthalein, and sildenafil.
Recalls & Warnings
November 21, 2013
Weight Loss Supplement Recalled
On November 14, 2013, Deseo Rebajar Inc. issued a recall of one lot of weight loss supplement Adipotrim XT because it was found to contain undeclared fluoxetine.
News Release
August 07, 2002
ConsumerLab.com finds some spoilage and inaccuracy among omega-3 and 6 supplements — List released of evening primrose, flaxseed and other GLA/ALA products that passed testing
WHITE PLAINS, NY — August 7, 2002 — ConsumerLab.com, an independent evaluator of health and nutrition products, released results today of its Product Review of Black Currant, Borage, Evening Primrose, and Flaxseed Oils: Sources of ALA and GLA (Omega-3 and -6 Fatty Acids).
News Release
July 16, 2002
ConsumerLab.com finds lead contamination remains a problem for certain mineral supplements — Lead found in iron, magnesium and, most recently, potassium pills
WHITE PLAINS, NY — July 16, 2002 — ConsumerLab.com announced today that its testing has shown that approximately 5% to 10 % of certain mineral supplements are contaminated with lead. The findings are based on ConsumerLab.
Recalls & Warnings
October 13, 2017
Hi-Tech To Pay Over 40 Million to Settle FTC Charges of False Claims
On October 11, 2017, a U.S. District Judge ruled that Hi-Tech Pharmaceuticals Inc.
Recalls & Warnings
September 28, 2017
Seller of Prostate, Reishi Supplements Warned for Manufacturing Violations
On September 11, 2017, the FDA issued a warning letter to Vicare International (USA), Inc.
Recalls & Warnings
August 29, 2017
FDA Warns Seller of Supplements for Allergies, Joint Pain, Bone Health, and More
On August 16, 2017, the FDA issued a warning letter to Total Nutrition, Inc.
Recalls & Warnings
August 01, 2017
FDA Warns Seller of Acai, Garcinia & More for Drug Claims
On July 25, 2017, the FDA issued a warning letter to Absonutrix, following a review of the company's website, www.absonutrix.com, which found statements made about some of its products to be drug claims.
Recalls & Warnings
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.
Recalls & Warnings
October 08, 2016
Seller of Cell Power and Super Silica Warned for Manufacturing Violations, Misbranding
On September 23, 2016, the FDA issued a warning letter to SSO, Inc.
Recalls & Warnings
September 27, 2016
Seller of B Vitamins, Omega-3s and More Warned for Manufacturing Violations, Drug Claims
On September 15, 2016, the FDA issued a warning letter to Positive Power Nutrition, following a facility inspection which found the company's products, including High Energy C-Complex, Positive Vitality, Positive Performance, Positive CardioGuard, B-Complex 100, Positive Essentials, Positive ...
Recalls & Warnings
September 14, 2016
Seller of Aloe, Prostate and Joint Supplements Warned for Manufacturing Violations
On April 8, 2016, the FDA issued a warning letter to Salud Natural Entrepreneurs, Inc.
Recalls & Warnings
September 07, 2016
Seller of Herbal Formulas for Cholesterol, Prostate & More Warned For Drug Claims
On July 29, 2016, the FDA issued a warning letter to Healing-Scents following a review of the company's website, which found statements made about its products, Heart Herbs, Cholesterol Regulation Herbs, Diabetes Regulation Herbs, Prostate Healer Herbs, High Blood Pressure Herbs, ...
Recalls & Warnings
September 06, 2016
Seller on Noni Juice Warned for Manufacturing Violations, Drug Claims
On August 26, 2016, the FDA issued a warning letter to Healing Noni Co. L.L.C.
Recalls & Warnings
August 31, 2016
Seller of Joint Supplement Warned for Manufacturing Violations, Drug Claims
On July 15, 2016, the FDA issued a warning letter to Vitalife Inc.
Recalls & Warnings
August 23, 2016
Seller of Aloe Liquid and Capsules Warned for Manufacturing Violations, Drug Claims
On July 15, 2016, the FDA issued a warning letter to Aloe Farms, Inc.
Recalls & Warnings
January 21, 2017
Seller of "Cancer Kits," Alpha Lipoic Acid Supplements and More Warned for Drug Claims
On December 22, 2016, the FDA issued a warning letter to Northern Health Products, Inc. following a review of the company's websites, www.northernhealthproducts.com and www.petdca.
Recalls & Warnings
January 17, 2017
Seller of Heart, Senior and Teen Supplements Warned For Drug Claims
On December 7, 2016, the FDA issued a warning letter to Esteem Products Ltd following a review of the company's website, which found statements made about its products, Cardio Life, Total Man, Total Woman, Senior Total Man, Senior Total Woman , and Total Teen to be drug ...
Recalls & Warnings
February 09, 2017
Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products
On February 9, 2017, the FDA announced that VivaCeuticals Inc, doing business as Regeneca Worldwide, has been ordered by a federal court to stop selling its products, which were found to contain unsafe ingredients including DMAA.
Recalls & Warnings
June 27, 2017
Seller of Alpha Lipoic Acid, Cinnamon Supplements and More Warned For Manufacturing Violations
On May 1, 2017 the FDA issued a warning letter to Nature's Vision, Inc.
Recalls & Warnings
June 07, 2017
FDA Warns Seller of Probiotic and Omega-3 Supplements for Manufacturing Violations
On May 22, 2017, the FDA issued a warning letter to BioTE Medical, LLC following a facility inspection which found its products, including BioTE DIM, BiotTE Probiotic, BioTE Iodine Plus, and BioTE Omega 3 to be adulterated because they were prepared, packed, or held under ...
Recalls & Warnings
June 06, 2017
Seller of Vision, Cholesterol, Prostate Supplements and More Warned for Drug Claims
On May 25, 2017, the FDA issued a warning letter to Herbal Doctor Remedies following a facility inspection and review of the company's websites, www.herb-doc.com, www.ChinaSecretMed.com and www.theraherb.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
February 17, 2015
Seller of Muscle Supplements Containing Synthetic Steroids Warned
On February 9, 2015, the FDA issued a warning letter to A2Z Industries, LLC, following a facility inspection which found the company's muscle enhancing supplements, including HaloV and EPI2A3A to be labeled as containing synthetic steroids.
Recalls & Warnings
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 ...
Recalls & Warnings
February 06, 2015
Seller of Aloe Supplement Warned for Drug Claims
On January 21, 2015, the FDA issued a warning letter to Pristine Nutraceuticals, LLC, following a review of the company's website, http://www.digestaqure.com, which found statements made about DigestaCure to be drug claims.
Recalls & Warnings
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.
Recalls & Warnings
August 08, 2014
FDA Warns Puerto Rico Supplement Seller
On June 30, 2014, the FDA issued a warning letter to Mr. Ramon Rosa, following a review of his website, www.aceitedeguanabana.
Recalls & Warnings
August 08, 2014
Weight Loss Supplement Found to Contain DMAA Recalled
On August 6, 2014, Regeneca Worldwide issued a recall of two lots of appetite control supplement RegenESlim because FDA tests found them to contain DMAA (1,3-dimethylamylamine).
Recalls & Warnings
September 02, 2014
Recall of Weight Loss Supplement Expanded
On August 27, 2014, Regeneca Worldwide expanded its previous recall of two lots of appetite control supplement RegenESlim to include two more lots because FDA tests found them to contain DMAA (1,3-dimethylamylamine).
Recalls & Warnings
October 21, 2015
Imported Supplements Can Be Dangerous, FDA Warns
On October 15, 2015, the FDA warned consumers that some supplements sold at nontraditional places, such as ethnic or international stores, flea markets, swap meets, as well as online, are often imported from other countries, and some can potentially be harmful.
Recalls & Warnings
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.
Recalls & Warnings
August 06, 2015
Children and Adult Gummy Vitamins Recalled in Canada Due to Excessive Vitamin D
On August 6, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced Church & Dwight Canada Corp. is recalling the following supplements because they contain more vitamin D than claimed on the label (identified in Canada by their assigned natural product number (NPN):
Recalls & Warnings
July 28, 2015
Abnormal Heart Rhythms Linked with Unauthorized Natural Product, Health Canada Warns
On July 27, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced that it has received a serious adverse reaction report of abnormal heart rhythms associated with the use of an unauthorized natural product in Canada called Remogen, which contains the drug ibogaine.
Recalls & Warnings
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.
Recalls & Warnings
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 ...
Recalls & Warnings
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.
Recalls & Warnings
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 ...
Recalls & Warnings
March 06, 2015
Seller of Tea Drinks Warned for Drug Claims
On February 26, 2015, the FDA issued a warning letter to the seller of Anamu CancerHerb Tea Box, Anamu CancerHerb Tea Box with Honey and Organic Bottled Tea Drinks because statements made about these products on the websites, www.cancerherbtea.com and www.anamucancerherbtea.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
January 20, 2016
Maker of Growth Hormone, Testosterone Booster Warned for Manufacturing Violations, Misbranding
On January 8, 2016, the FDA issued a warning letter to Nutraloid Labs Inc.
Recalls & Warnings
January 20, 2016
Seller of Aloe, Moringa Supplements Warned for Manufacturing Violations, Drug Claims
On January 13, 2016, the FDA issued a warning letter to Alkebulan International Services, LLC, following a facility inspection which found the company's products,Aloe Ferox and Moringa Oleifera Capsule to be adulterated because they prepared, packed, or held under conditions that ...
Recalls & Warnings
January 16, 2016
Seller of Liver, Lung Support Supplements Warned for Drug Claims
On January 4, 2016, the FDA issued a warning letter to Tibetan Herbal Balance, Inc.
Recalls & Warnings
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 ...
Recalls & Warnings
July 23, 2016
Maker of "Super Food" Warned for Manufacturing Violations
On July 12, 2016, the FDA issued a warning letter to TerraVare, Inc.
Recalls & Warnings
May 24, 2016
Seller of Joint Health, Omega-3 Supplements & More Warned for Manufacturing Violations, Drug Claims
On May 13, 2016, the FDA issued a warning letter to Rocky Fork Formulas, Inc.
Recalls & Warnings
August 02, 2016
Seller of Whey Protein Warned for Manufacturing Violations, Drug Claims
On July 22, 2016, the FDA issued a warning letter to New Horizon Nutraceuticals, LLC, following a facility inspection which found the company's product, One World Whey Protein Power Food to be adulterated because it was prepared, packed, or held under conditions that violate Current ...
Recalls & Warnings
May 15, 2016
Seller of Vision Supplements Warned for Drug Claims
On April 28, 2016, the FDA issued a warning letter to Macular Health, LLC.
Recalls & Warnings
January 26, 2016
Seller of CoQ10, SAM-e, Vitamin D, and More Warned for Manufacturing Violations, Drug Claims
On January 15, 2016, the FDA issued a warning letter to Nutri-Dyn Midwest, Inc., following a facility inspection which found the company's products, including Cardioauxin BP, Zinc Lozenge, Oliver, Pau D'Arco, Petadolex, Chondro Jointaide, Dynagesic, SAMe-200, Gugulipid.
Recalls & Warnings
February 06, 2016
Seller of Turmeric, Milk Thistle and More Warned for Manufacturing Violations, Drug Claims
On January 15, 2016, the FDA issued a warning letter to Terra Firma Botanicals, Inc.
Recalls & Warnings
March 08, 2016
Seller of Echinacea Warned Manufacturing Violations, Drug Claims
On February 25, 2016, the FDA issued a warning letter to Herbal Energetics/ In Joy Organics, following a facility inspection which found the company's product, X Out-Rays to be adulterated because it was prepared, packed, or held under conditions that violate Current Good ...
Recalls & Warnings
June 23, 2003
FDA Warns Consumers Against Taking 6 Sexual Enhancement Supplements
On June 20, 2003, the Food and Drug Administration (FDA) warned consumers not to purchase or consume the following products: SIGRA, STAMINA Rx and STAMINA Rx for Women, Y-Y, Spontane ES and Uroprin, manufactured by NVE, Inc., in Newton, N.J. and distributed by Hi-Tech in Norcross, Ga.
Recalls & Warnings
July 27, 2012
Prescription and Street Drug Alternatives Found in Male Enhancement, Mood, and Sleep Supplements
On July 10, 2012, the FDA issued a warning letter to Evol Nutrition Associates, Inc. subsequent to a 2011 inspection which found a number of the company's products contained prescription and investigational drugs and were misbranded.
Recalls & Warnings
March 25, 2008
FDA Warns of Sexual Supplements with Drug-like Ingredients
On March 25, 2008, the U.S. Food and Drug Administration advised consumers not to purchase or use "Blue Steel" or "Hero" products marketed as dietary supplements throughout the United States because they are considered unapproved drugs and have not been proven to be safe or effective.
Recalls & Warnings
July 29, 2008
Recall of Sexual Enhancement Supplements Containing Drug
On July 28, 2008 the U.S. FDA announced that Jack Distribution, LLC and G & N works, Inc. are conducting a voluntary nationwide recall of all lot numbers of the company's supplement products sold under the brand names Rize 2 The Occasion and Rose 4 Her.
Recalls & Warnings
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.
Recalls & Warnings
June 16, 2004
FTC Challenges Ads for Kids’ Weight Loss Pill and Female Sexuality Supplement
On June 16, 2004 The Federal Trade Commission announced that it had charged three Florida-based companies and their principals with making false and unsubstantiated claims in connection with the advertising for “Pedia Loss,” a purported children’s weight loss product.
News Release
June 25, 2002
ConsumerLab.com reviews radioprotective Iodine pills in response to terrorist threats — Quality of products is high, but local access is poor
WHITE PLAINS, NY — June 25, 2002 — In response to the threat of terrorist attacks on U.S. nuclear facilities, ConsumerLab.com, an evaluator of health and nutrition products, today released a Product Review of Potassium Iodide/Potassium Iodate (Radioprotective Agents).
Recalls & Warnings
July 28, 2008
Seizure of Xiadafil VIP Tablets After Company Refuses Recall
On July 24, 2008, the FDA announced that U.S. Marshals seized nearly $74,000 worth of Xiadafil VIP tablets, Lots 6K029 and 6K209-SEI, distributed by SEI Pharmaceuticals, Inc. of Miami, Fla.
Recalls & Warnings
June 15, 2009
Sexual Enhancement Supplement Recalled -- Second Time Found with Drug-like Compound
On June 15, 2009, the U.S. FDA announced that, per its order, Hi-Tech Pharmaceuticals, Inc. is conducting a nationwide voluntary recall of the company's product sold under the name Stamina-Rx.
Recalls & Warnings
May 10, 2007
FDA Warns of Two Supplements Containing Pharmaceutical-like Compounds
On May 10, 2007, the FDA advised consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States.
Recalls & Warnings
December 21, 2016
Seller of 5-HTP, Chromium, Curcumin and More Warned for Drug Claims
On December 1, 2016, the FDA issued a warning letter to Aurora Health and Nutrition following a review of the company's website, which found statements made about its products, 5-HTP, Alpha Lipoic Acid, the Argentyn 23 product line, Artecin 90 Vegetarian Capsules, ...
Recalls & Warnings
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 ...
Recalls & Warnings
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, ...
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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 ...
Recalls & Warnings
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, ...
Recalls & Warnings
August 02, 2014
Judge Orders BioAnue To Stop Illegal Cancer and Disease Claims
On July 23, 2014, Gloria D.
Recalls & Warnings
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.
News Release
May 15, 2002
ConsumerLab.com lists magnesium products that passed testing — Some products fail due to excess magnesium and lead contamination
WHITE PLAINS, NY — May 14, 2002 — ConsumerLab.com today released results of its Product Review of Magnesium Supplements. Seventeen of the nineteen products tested by ConsumerLab.com passed the review. Among the products that failed, one contained nearly 50% more magnesium than claimed.
Recalls & Warnings
June 13, 2013
Seller of Cardio, Immune, Greens Supplements and More Warned For Drug Claims
On May 29, 2013, the FDA issued a warning letter to dietary supplement company Nature's Answer, following a review a the company's website, www.naturesanswer.
Recalls & Warnings
May 28, 2008
FDA Requests Recall of Xiadafil VIP Supplements
On May 27, 2008, the U.S. The U.S. Food and Drug Administration announced that it had requested that SEI Pharmaceuticals, of Miami, Fla.
News Release
April 16, 2002
ConsumerLab.com finds "Breast Enhancement" pills lack evidence of efficacy
WHITE PLAINS, NY — April 16, 2002 — ConsumerLab.com announced today that it found no hard evidence to suggest that current dietary supplements marketed for breast enhancement are effective.
Recalls & Warnings
September 26, 2020
Cognitive Enhancement Supplements Can Contain Unapproved Drugs
Recent testing detected five unapproved drugs in 10 over-the-counter cognitive enhancement and workout supplements sold in the US.
Recalls & Warnings
July 31, 2018
FDA Warns Seller of Joint Health and Cholesterol Supplements
On July 13, 2018, the FDA issued a warning letter to GC Natural, following a facility inspection which found a number of the company's products, including Red Pyrola Plus + Advanced Joint Formula Capsules, CSDP GOLD Capsules, Rejeune Optimal Kidney & Liver Support Extract balls, C.
Recalls & Warnings
April 09, 2006
Sellers of Children’s Weight-Loss Product Settle FTC Charges
On April 6, 2006, the Federal Trade Commission (FTC) announced that the marketers of Pedia Loss, a purported children’s weight-loss product, and Fabulously Feminine, a supposed female libido enhancement product, had agreed to settle Federal Trade Commission charges that they made false and ...
Recalls & Warnings
November 26, 2019
Cognitive Enhancement Supplements Contain Unapproved Drug
Several supplements sold in the U.S. and promoted for cognitive enhancement contain significant amounts of the drug piracetam -- a drug that is not approved for use in the U.S. -- according to a study published this week in JAMA Internal Medicine.
Recalls & Warnings
May 29, 2021
FDA, FTC Warns Five Sellers of "Infertility" Supplements
The FDA and FTC (Federal Trade Commission) sent warning letters to the following five companies in May for illegally selling dietary supplements promoted with claims to treat infertility and other reproductive health issues:
Recalls & Warnings
June 25, 2020
"Anti-Viral" Supplement Recalled for Unsupported Coronavirus Claims
On June 23, 2020, Golden Nutrition Inc. issued a recall of four lots of Anti-Viral Immune Enhancement Capsules because the label makes unsupported health claims to "help fight corona virus and influenza.
Recalls & Warnings
April 21, 2012
FDA Finds Prescription Drug Analog in 3 Enhancement Supplements
On April 20, 2012, the U.S. FDA advised consumers not to purchase or use the following supplements from Enhance Nutraceutical: "Instant Hard Rod," "RigiRx Plus," and "Zen Maxx." FDA laboratory analysis confirmed that each contains aminotadalafil.
Recalls & Warnings
February 15, 2013
FDA Seizes Weight Loss Supplements Containing Undeclared Drug
On Feb. 14, 2013, U.S. Marshals acting on behalf of the FDA seized weight loss supplements from Globe All Wellness, LLC which were found to contain the undeclared drug sibutramine hydrochloride.
Recalls & Warnings
July 19, 2011
Recall of Enhancement Supplement for Men - Contains Drug Compounds
On July 13, 2011, Global Wellness, LLC announced an expanded voluntary nationwide recall of Via Extreme Ultimate Sexual Enhancer Dietary Supplement for Men. The product was distributed throughout the U.S. Puerto Rico, Barbados, and Canada to internet and retail consumers.
Recalls & Warnings
March 17, 2004
Marketers of “Focus Factor” and “V-Factor” Fined for Advertising Claims
On March 17 , 2004 the Federal Trade Commission (FTC) reported that the marketers of “Focus Factor,” a dietary supplement that purports to improve concentration, and “V-Factor,” a supplement that purports to enhance sexual performance, have agreed to settle charges that they made numerous ...
Recalls & Warnings
August 13, 2010
Recall of Male Enhancement Supplement Sold in National Stores
On August 9, 2010 the U.S. FDA announced that the company Prolatis' of Salt Lake City, Utah is conducting a voluntary recall of the company's product sold as Prolatis'.
Recalls & Warnings
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.
Recalls & Warnings
October 24, 2012
FDA Seizes Many Supplements from New York Company Due To Drug Claims
On October 23, 2012, U.S. Marshalls, acting on behalf of the FDA, seized dietary supplements and unapproved drugs from Confidence, Inc., a supplement manufacturer in Port Washington, N.Y. The products included dietary supplements Dr.
Recalls & Warnings
August 31, 2004
Two Makers of Weight Loss and Sex Enhancement Supplements Stopped From Making Unsubstantiated Claims
On August 27, 2004, the Federal Trade Commmission (FTC) reported that two Maine-based dietary supplement marketers and their principals have agreed to settle FTC charges that they made deceptive advertising claims about their dietary supplement products, in violation of federal law.
Recalls & Warnings
May 12, 2018
Seller of Maca Powder Warned for Drug Claims
On April 18, 2018, the FDA issued a warning letter to Herbs America, Inc. following review of the company's website, and the company's Maca Magic store on www.amazon.
Recalls & Warnings
June 20, 2019
Weight Loss, Muscle & Energy Supplements Linked to Adverse Events in Children and Young Adults
Consumption of dietary supplements sold for weight loss, muscle building, and energy are associated with an increased risk for severe medical events in children and young adults compared to the consumption of vitamins, according to a recent study published in the Journal of the Adolescent ...
Recalls & Warnings
September 25, 2018
Seller of B Vitamins, Multis, Glucosamine & More Warned for Manufacturing Violations
On August 31, 2018, the FDA issued a warning letter to Independent Nutrition Inc., following a facility inspection which the company's products, including B-50 Complete, Multi-Vitamin & Mineral Complex (a.k.a.
Recalls & Warnings
September 25, 2018
FDA Warns Seller of Digestive Enzyme Supplements
On March 6, 2018, the FDA issued a warning letter to Uckele Health & Nutrition, Inc.
Recalls & Warnings
November 25, 2007
Recall of Men's "Sexual Energy" Supplement Expanded to Include "Energy Max" Product
On November 16, 2007, American True Man Health Incorporated announced that it is expanding it's voluntary recall of the Company's dietary supplement product sold under the name and identified as True Man's Sexual Energy Nutriment Men's Formula with the expiration date up to and including December ...
Recalls & Warnings
May 20, 2017
Muscle Enhancement Supplement Containing Steroid-Like Substances Recalled
On May 19, 2017, Dynamic Technical Formulations LLC issued a recall of all lots its muscle enhancement supplement Tri-Ton because it was found to contain anabolic steroid-like substances (andarine and ostarine) which are not permitted in dietary supplements.
Recalls & Warnings
July 10, 2017
Bodybuilding Supplements Containing Steroid-Like Substances Recalled
On June 29, 2017, Hardcore Formulations recalled all lots and expiration dates of their products Ultra-Sten and D-Zine, bodybuilding supplements found to contain methylstenbolone and dymethazine, which are derivatives of anabolic steroids.
Recalls & Warnings
January 13, 2018
Seller of Depression, Prostate Supplements & More Warned for Manufacturing Violations, Drug Claims
On August 21, 2017, the FDA issued a warning letter to Irmo-Vita, LLC, following a facility inspection which found that several of the company's products, including Hysta-Min, Man-Affirm, Phung-EX, and Bacto- EX to be adulterated because they were prepared, packed, or held ...
Recalls & Warnings
May 08, 2017
Muscle Enhancement Supplement Recalled
On May 5, 2017, Genetic Edge Compounds issued a recall of all lots its muscle enhancement supplement GEC Laxoplex because FDA analysis found it to contain anabolic steroids and steroid like substances, which are not permitted in dietary supplements.
Recalls & Warnings
November 14, 2014
FDA Warns Consumers Not to Buy or Use Muscle Enhancement Supplement
On November 13, 2014, the FDA advised consumers not to buy or use the muscle enhancement supplement Mayhem (Chaotic-Labz) because it was found to contain the undeclared drugs cyproheptadine and dexamethasone. These drugs can cause serious side effects and can interact with other medications.
Recalls & Warnings
October 14, 2015
No Vinpocetine in Some Vinpocetine Supplements; Picamilon Labels Not Accurate
A recently published study of 23 supplements listing vinpocetine as an ingredient found six did not contain any vinpocetine. Among those that did contain vinpocetine, most did not list amounts on the label, but amounts found in suggested daily servings varied by almost 100-fold, from 0.
Recalls & Warnings
April 05, 2016
Muscle Enhancement Supplement Recalled
On April 5, 2016, Invisiblu International LLC issued a recall of one lot of the muscle enhancement supplement Continuum Labs LGD-Xtreme because it contains LGD-4033 Ligandrol. The risks of this ingredient are not known.
Recalls & Warnings
April 08, 2010
Capsule for Men Spiked with Erectile Drug
On April 7, 2010, the U.S.
Recalls & Warnings
September 13, 2010
Supplement for "Increasing Desire" Recalled for Containing Drug
The U.S. FDA posted a notice regarding the recall of Masxtreme Capsules by the distributor, Natural Wellness, Inc. FDA analysis has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil.
Recalls & Warnings
January 16, 2013
Nutrition Bars Recalled Due To Undeclared Allergen
On January 15, 2012, Belmont Confections Inc. issued a voluntary recall of Dymatize Nutrition Elite Gourmet Cookies & Cream bars and Dymatize Nutrition Elite Gourmet Fudge Brownie bars because they may contain undeclared peanuts.
Recalls & Warnings
July 05, 2012
FDA Warns Good Herbs Inc. of Manufacturing Violations and Drug Claims
The FDA issued a warning letter to Good Herbs Inc. on May 24, 2012, after a facility inspection found the company to be in violation of current manufacturing regulations, including lack of documentation and written procedures.
Recalls & Warnings
October 21, 2014
Seller of Weight Loss, Saw Palmetto Supplements and More Warned for Drug Claims
On October 9, 2014, the FDA issued a warning letter to Bethel Nutritional Consulting, Inc., following a review of the company's website which found statements made about 15 Day Detox Diet, Alpha Lipoic Acid. 300 mg.
Recalls & Warnings
December 05, 2015
FDA Warns Companies Selling Products Containing Picamilon
On November 30, 2015, the FDA issued warning letters to five supplement companies selling products containing picamilon, which is not a lawful dietary supplement ingredient in the U.S.
Recalls & Warnings
February 15, 2013
Energy Drink Recalled Due To Bacterial Contamination
On December 21, 2012, NBTY issued a voluntary recall of the energy supplement MET-Rx Extreme Thermo Rage Watermelon 8 fl. oz. (Manufactured by MET-Rx Nutrition, Inc.) due to bacterial contamination.
Recalls & Warnings
October 22, 2010
Enzyte "Male" Supplement Found to Affect Heart
The journal Archives of Internal Medicine (August 2010) includes a report of a small clinical trial of the dietary supplement Enzyte, which is marketed for "male enhancement."
Recalls & Warnings
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.
Recalls & Warnings
July 30, 2008
Recall of Viapro Capsules Due to Potentially Harmful Ingredient
The U.S. FDA has posted a release noting that EG Labs, LLC announced a nationwide voluntary recall on July 23, 2008 of all lots of its supplement product sold under the brand name, Viapro, in 375mg capsules.
Recalls & Warnings
May 29, 2008
Recall of Virility Supplement
On May 29, 2008, the FDA posted a recall by International Pharmaceuticals, Ltd. of all of the company's supplement sold under the name of Viril-Ity-Power (VIP) Tabs, 560mg/serving.
Recalls & Warnings
March 04, 2008
Two Supplements Recalled for Containing Viagra-like Compounds
On March 4, 2008, the FDA posted a release from Palo Alto Labs (dated February 28) announcing a voluntary nationwide recall of the company's supplement products sold under the name Aspire36 and Aspire Lite.
Recalls & Warnings
November 26, 2007
Encore Tabs Recalled -- Contain Prescription Drug
On November 21, 2007, Bodee LLC announced today that it is conducting a voluntary nationwide recall of all the company's supplement product sold under the name Encore Tabs.
Recalls & Warnings
February 24, 2011
Recall of Counterfeit Extenze Tablets Containing Drugs
On February 23, 2011, the FDA announced that Biotab Nutraceuticals, Inc. was notified that two lots of counterfeit product purporting to be Extenze contain undeclared drug ingredients. Specifically, lot 0709241 contains tadalafil and sildenafil, and lot 0509075 contains tadalafil and sibutramine.
Recalls & Warnings
January 01, 2011
Recall of Two Supplements Spiked with Erectile Dysfunction Drug
On December 22, 2010 the U.S.
Recalls & Warnings
September 12, 2010
Mr. Magic Male Enhancer Recalled
The U.S. FDA posted a recall announcement daated August 18, 2010 from Glow Industries regarding "Mr. Magic Male Enhancer from Don Wands.
Recalls & Warnings
April 07, 2010
Nationwide Recall of Masxtreme Capsules Containing Drugs with Cardiovascular Side Effects
On March 30, 2010, the U.S. Food and Drug Administration (FDA) posted a notice from Natural Wellness warning consumers not to purchase or consume the product known as MasXtreme, Lot# 911035.
Recalls & Warnings
February 13, 2013
FDA Warns Maker of Weight Loss and Whey Protein Supplements For Manufacturing Violations and Misbranding
January 25, 2013, the FDA issued a warning letter to dietary supplement manufacturer SciLabs Nutraceuticals, following a facility inspection which found the company's dietary supplements and supplement ingredients, including N-Large 2, Flo-Gard AB, Nitrogen Glutamine capsules, Nutritech nutritional ...
Recalls & Warnings
November 02, 2012
Maker of Joint Health, Blood Sugar, Prostate, Ginkgo Supplements and More Warned For Drug Claims, Misbranding and Adulteration
On September 10, 2012, the FDA issued a warning letter to Global Source Management & Consulting for making drug claims about the following dietary supplements: Scientific Joint Program capsules, Alpha Lipoic Acid, Healthy Blood Sugar Diabetic Support, Dr.
Recalls & Warnings
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 ...
Recalls & Warnings
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 ...
Recalls & Warnings
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 ...
Recalls & Warnings
February 13, 2014
Maker of Cholesterol and Workout Supplements Warned For Manufacturing Violations, Drug Claims and Unapproved Ingredient
On January 31, 2014, the FDA issued a warning letter to Exclusive Supplements Inc.
Recalls & Warnings
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.
