Product Reviews and Information for Fertility (Male & Female)
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CL Answer
Can taking astaxanthin increase the risk of breast enlargement in men?
Find out if taking astaxanthin can increase the risk of breast enlargement (gynecomastia) in men.
CL Answer
Which supplements may help with PCOS (polycystic ovarian syndrome)?
Many supplements are promoted to help treat symptoms of PCOS (polycystic ovarian syndrome), but do they really work? See the clinical evidence for inositol (myo-inositol and D-chiro-inositol), alpha lipoic acid, vitamin B-12, folic acid, vitamin D and more.
CL Answer
Do hair loss supplements, such as Viviscal, Hair La Vie, and Nutrafol, or topical essential oils work?
Vitamins and supplements that may help with hair loss and thinning, including saw palmetto, beta-sitosterol, protein, iron, and vitamin D.
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
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.
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
May 01, 2025
Male Enhancement Supplements Recalled
On April 25, 2025, Health Fixer recalled all lots of Male Ultra, Malextra, Electro Buzz, Ultra Armor and Male Ultra Pro supplements because laboratory analysis found them to contain chloropretadalafil, propoxyphenylsildenafil, and sildenafil, drugs that are not permitted to be ...
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
February 24, 2025
Vitality Sexual Enhancement Supplement Recalled
On February 20, 2025, One Source Nutrition recalled all lots of Vitality capsules after FDA analysis found the supplements to contain undeclared prescription drugs sildenafil and tadalafil, which are not permitted in dietary supplements.
Recalls & Warnings
February 27, 2025
Male Enhancement Supplement Sold on Amazon and Walmart Recalled
On February 25, 2025, Natural Dior LLC recalled affected lots of a dietary supplement Vitafer-L Gold Liquid because it contains undeclared tadalafil, which is not permitted in dietary supplements.
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
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
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.
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
March 08, 2007
FTC Files Against Maker of Calcium and Fertility Supplements
On January 29, 2007, the Federal Trade Commission (FTC) announced that it had filed civil contempt charges against Lane Labs, Inc.
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 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
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
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
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
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
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
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
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
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.
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
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
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
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
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
January 04, 2020
Hormonal Balance Supplement Tied to Liver Failure
An otherwise healthy 23-year old woman in Texas is reported to have recently developed liver failure (requiring a liver transplant) after taking the supplement Balance (from Alani Nu) for four months.
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
January 12, 2021
FDA Warns Seller of Joint and Hair Loss Products
On December 22, 2020, the FDA issued a warning letter to Speedwinds Nutrition, Inc. following a review of the company's website, which found statements made about the company's products Synotrex and Sephren to be drug claims.
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
November 06, 2014
Seller of Prostate, Heart Supplements and More Warned for Drug Claims
On October 9, 2014, the FDA issued a warning letter to Health Research Laboratories, LLC/New World Health, following a review of the company's websites, which found statements made about AtheChel Advanced, Betarol, BioTherapex, Omega-3 Cardio Plus, RejuvaLifeRx, and Ultimate Health Formula to be ...
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
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
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
May 20, 2015
Supplements to Eliminate Gray Hair Not Supported by Science, Says FTC
On May 13, 2015, the FTC announced marketers of GetAwayGrey and Rise-N-Shine, dietary supplements promoted to reverse or prevent gray hair, have agreed to settle charges that claims made about the products are not supported by science.
Recalls & Warnings
May 16, 2015
FTC Mails Refund Checks to Nopalea Consumers
On May 15, 2015, the FTC announced it is mailing almost 500,000 checks totaling approximately $3 million to consumers who purchased the cactus-based fruit drink Nopalea (TriVita Inc).
Recalls & Warnings
May 13, 2015
Amberen Weight Loss Claims Not Supported by Evidence, Says FTC
On May 12, 2015, the FTC announced it filed a complaint to stop Lunada Biomedical Inc. from advertising that its product Amberen is clinically proven to cause substantial weight loss in women over 40.
Recalls & Warnings
May 09, 2015
Marketers Charged with Using Stolen Email Accounts to Promote Weight Loss Supplements Temporarily Shut Down
On May 4, 2015, the FTC announced it has obtained a court order to temporarily halt the operations of weight loss marketers Sale Slash, charging that the company used affiliate marketers to send illegal spam emails and post banner ads online that led consumers to fake news sites.
Recalls & Warnings
March 24, 2015
FTC Mails Refund Checks for Calcium Supplements
On March 18, 2015, the FTC announced 17,606 refund checks, totaling $954,828 were mailed to consumers who purchased the calcium supplement AdvaCAL (Lane Labs).
Recalls & Warnings
July 12, 2015
Marketers of Memory Supplement to Pay $1.4 Million to Settle FTC Charges
On July 8, 2015, the FTC announced the marketers of Procera AVH (Brain Research Labs Inc.) have agreed to pay $1.4 million to settle charges they made deceptive claims that the supplement could significantly improve memory, mood and cognitive function.
Recalls & Warnings
February 06, 2016
Marketers of Weight Supplements AF Plus and Final Trim Violated Consumer Protection Laws, Says FTC
On January 19, 2016, the Federal Trade Commission (FTC) and State of Maine's Office of the Attorney General charged marketers of weight loss supplements AF Plus and Final Trim with violating consumer protection laws.
Recalls & Warnings
February 05, 2016
Garcinia, Green Coffee Marketers Pay $43 Million to Settle Charges of False Weight Loss Claims
Sale Slash, LLC, has agreed to pay more than $43 million to settle FTC charges it used unsubstantiated claims and fake celebrity endorsements to promote its Premium Green Coffee, Pure Garcinia Cambogia, Premium White Kidney Bean Extract, Pure Forskolin Extract, and Pure Caralluma Fimbriata Extract ...
Recalls & Warnings
April 28, 2017
Marketers of Weight Loss System Agree to Settle FTC Charges of Deceptive Claims
On April 21, 2017, the FTC announced the marketers of the NutriMost Ultimate Fat Loss System (NutriMost, LLC and NutriMost Doctors, LLC) agreed to settle charges they made false claims about the product.
Recalls & Warnings
October 11, 2016
Seller of Glucosamine and Chondroitin Settles FTC Charges of False Advertising
On October 5, 2016, the FTC announced the sellers of the liquid glucosamine and chondroitin supplement Supple (Supple LLC) agreed to settle charges they made false claims about the product.
Recalls & Warnings
October 01, 2016
No Evidence Supplement Can Reverse or Prevent Gray Hair, Says FTC
On September 23, 2016, the FTC announced a U.S. district court has issued a judgement prohibiting the makers of Grey Defence dietary supplements from making claims the products can reverse or prevent grey hair, unless they are not misleading and are supported by reliable scientific evidence.
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
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
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 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
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.
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
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
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 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
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
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
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
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
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
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
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
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
December 01, 2017
Health Research Labs Agrees to Settle FTC Charges of False Claims, Deceptive Marketing of BioTherapex and NeuroPlus
On November 30, 2017, the FTC announced Health Research Laboratories LLC and owner, Kramer Duhon, agreed to settle charges that they made false claims about the company's products, BioTherapex and NeuroPlus.
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.
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
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
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
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
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
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
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
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
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
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
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
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
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
January 07, 2002
Liver Toxicity with Kava
As announced in a December 19, 2001 letter to healthcare professionals, The Food and Drug Administration (FDA) is investigating whether the use of dietary supplements containing kava (also known as kava kava or Piper methysticum) is associated with liver toxicity.
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
October 18, 2017
FDA Warns Seller of Arthritis, Blood Pressure, Diabetes Supplements For Making Drug Claims
On August 15, 2017, the FDA issued a warning letter to Years to Your Health, Inc., following an inspection of the company's website which found a number of their products to be misbranded, as they contained drug claims.
