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Sexual Enhancers

Find the best sexual enhancement supplements with ingredients such as yohimbe, horny goat weed, and arginine. Review evidence for these ingredients and their use for sexual dysfunction and increasing sex drive. Review dosage info, safety, side effects and potential drug interactions.

Sexual Enhancers Review

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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.

Couple 1400

Product Review

Maca Supplements Review

Choose the Best Maca Supplement. Make Sure Your Maca Supplement Isn't Contaminated With Lead.

Maca Supplements Reviewed by ConsumerLab.com

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?

Man Holding Blister Packs of Supplements

Product Review

L-Arginine Supplements Review

Choose the Best L-Arginine Supplement. Find Out Which L-Arginine Supplement Passed CL's Tests.

L-Arginine Supplements Reviewed by ConsumerLab.com

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.

Man in Grey Tee Holding Water and White Supplement

Product Review

Ginseng Supplements Review

Find the Best Ginseng Supplement. Key "Ginsenosides" Found to Range 10-Fold Across Products.

Ginseng Supplements Reviewed by ConsumerLab

Product Review

Ashwagandha Supplements Review

Find the Best Ashwagandha Supplement. Only 56% of Ashwagandha Products Pass Tests.

Ashwagandha supplements reviewed by ConsumerLab.com

Product Review

DHEA Supplements Review

Choose the Best DHEA Supplement. Beware of Big Differences in Dose and Price.

DHEA Supplements Tested by ConsumerLab.com

News Release

September 11, 2017

ConsumerLab.com Tests L-Arginine "Blood Flow" Supplements, Identifying Its Top Picks

White Plains, New York, September 11, 2017 — L-arginine supplements are often promoted to increase exercise endurance, reduce symptoms of congestive heart failure and other cardiovascular conditions, and improve sexual function.

CL Answer

10 Supplements That May Boost Testosterone (And 11 That May Not)

Many supplements promise to increase testestorone, boost libido, and increase muscle size, but, as ConsumerLab explains, the actual effectiveness of supplements is limited, and some supplements may actually reduce testosterone levels.

Chalkboard sign that says low testosterone sitting on a table in front of a book and supplements

News Release

April 04, 2017

ConsumerLab.com Reveals Best and Worst Turmeric and Curcumin Supplements & Spices -- 31% Fail ConsumerLab.com Tests of Quality

White Plains, New York, April 4, 2017 — Turmeric and its key compound, curcumin, may be help reduce symptoms of inflammation in rheumatoid arthritis and osteoarthritis and may be helpful in treating depression, diabetes, and indigestion.

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.

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 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

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

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

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

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

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

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

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:

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.

Man taking blood pressure

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

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 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

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 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

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

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

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

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

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

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

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

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

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

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 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

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.

CL Answer

Are supplements which claim increased absorption or improved bioavailability telling the truth? Is it worth paying more for these? Are there concerns?

Learn more about bioavailability enhancers, including emulsifiers and enzyme inhibitors.

Enhancers in Supplements

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

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.

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

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

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

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

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.

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.

Product Review

Melatonin Supplements Review

Trouble Sleeping? See CL's Tests of Melatonin Supplements and Top Picks.

Melatonin Review 2024

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

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

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

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

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

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

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 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

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

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

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

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

September 04, 2018

Federal Court Shuts Down Maker of Sexual Enhancement Products

On August 30, 2018, the FDA announced that U.S.

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

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

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.

CL Answer

I have heard that caffeine can interfere with the benefits of creatine supplementation. Is that true?

Find out if creatine supplements are impacted by caffeine intake.

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

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. 

Product Review

Cranberry Juices and Supplements Review

CL's Tests Show Which Cranberry Juices and Supplements Are Best and Cost the Least

CL Answer

I read that sterol supplements to lower cholesterol like CholestOff can block the absorption of vitamins. Is that true?

Find out if CholestOff and other sterol supplements can block vitamin absorption in the body and other safety concerns.

Elderly Man Reading Supplement Bottle

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

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

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

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

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

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

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

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

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

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.

CL Answer

Now that it was shown that Ginkgo biloba is not an effective memory enhancer, are there any other health enhancing benefits from taking it, and, if so, what dose should one take daily?

Find out what Ginkgo Biloba can and can't do. Find out the health benefits and correct daily dosage.

Gingko Biloba Leaves and Supplements

CL Answer

Can I take CoQ10 at the same time as my statin, or should I take them separately?

Taking CoQ10 and statins (such as lovastatin and simvastatin)? Find out if you can take them at the same time or if they should be taken separately. ConsumerLab.com's answer explains.

Elderly Individual Taking Two Supplements from Blister Packs

CL Answer

Can turmeric or curcumin with black pepper extract cause constipation? I had this problem, but it resolved when I switched to a curcumin supplement without piperine (black pepper extract).

Learn more about black pepper extract, why it is added to turmeric/curcumin supplements, and if it can cause gastrointestinal effects.

Turmeric or Curcumin

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

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 >>

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.

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.

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

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

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

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

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.

CL Answer

I've heard that grapefruit juice can interact with medications because it inhibits an enzyme that breaks down drugs in the body. Do any supplements interact the same way with drugs?

CYP3A4 inhibitors, such as grapefruit, can interact with certain medications by inhibiting the liver enzyme that metabolizes many drugs. ConsumerLab.com's answer explains.

Grapefruit Juice, CYP3A4 and Supplement Interactions -- glass of grapefruit juice and grapefruit halves

CL Answer

What do alkaline booster drops do? Do they provide the same benefits as Kre-Alkalyn?

Learn more about alkaline drop supplements and what booster drops and KreAlkalyn are marketed to do.

Oil Drops On White Table Against Blue Background

CL Answer

What is the difference between cysteine and cystine?

Find out the difference between cysteine and cystine amino acids, including where each is found and their functions.

Young Woman Taking Supplement

CL Answer

What are human growth hormone (HGH) supplements? What are the benefits? Are they safe?

Learn about the benefits and risks of human growth hormone (HGH) supplements and injections. Get science-based insights on usage and effects.

Man at gym taking supplement

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. 

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 ...

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.

Supplements for Hair Loss -- woman looking at hairbrush

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

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

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

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

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

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

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

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 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

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

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

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

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

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

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

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.

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

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

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

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

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: 

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.

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.

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 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 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

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

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

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

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

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

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 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.

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.

Clinical Update

3/05/2024

Problems with Creatine

Recent tests of lesser-known brands of creatine gummies revealed that half contained little creatine and/or had impurities. Get the details by brand in our Muscle Enhancers Supplements Review. Also see our Top Picks among creatine supplements.

Clinical Update

9/04/2018

Glutamine for IBS?

Glutamine, an amino acid, plays a role in maintaining the digestive tract. Can taking it as a supplement help people with irritable bowel syndrome (IBS)? Find out what a recent study showed in the Glutamine section of the Muscle Enhancers Review.

Clinical Update

3/21/2020

CoQ10 Bioavailability

CoQ10 is not well absorbed unless taken with fats or oils, such as with a meal. Bioavailability-enhanced formulations allow CoQ10 to be taken without a meal, but how good are they? We've added new information about one such formula and how it compares to taking regular CoQ10 in the Absorption and Bioavailability Enhancers section of the CoQ10 and Ubiquinol Supplements Review. Also see our Top Picks for CoQ10 and ubiquinol.

Clinical Update

1/24/2016

Leucine Protects Muscle In Middle-Aged

A recent study found that active, middle-aged people restricted to bed rest for several days lost significantly less muscle mass and function if given a leucine supplement along with their meals. Fat gain was also reduced. Get the details, including our tests of leucine-containing supplements, in the Muscle Enhancers Review >>

Clinical Update

5/19/2013

Creatine for Fibromyalgia

A new study shows that creatine might have a role in boosting muscle strength in patients with fibromyalgia. Get the details, plus quality ratings for creatine supplements in our updated Muscle Enhancers (Creatine and Branched Chain Amino Acids) Review >>

Clinical Update

11/10/2013

Amino Acids Speed Recovery From Knee Surgery

A study of men and women receiving knee replacement surgery showed that taking essential amino acids (including branched-chain amino acids) twice daily before and after surgery reduced muscle loss and speeded recovery. For details, including dosage, plus our reviews of amino acid supplements, see the updated Muscle Enhancers Review >> 

Clinical Update

2/17/2015

Creatine Tested for Parkinson Disease

Taking creatine daily for at least five years did not slow the progression of Parkinson disease according to a recently reported study involving nearly 1,000 patients. For more details about the study, other studies with creatine (for strength, fibromyalgia, etc.), and our tests of creatine supplements, see the Product Review of Muscle Enhancers (Creatine and Branched-chain Amino Acids) >> 

Clinical Update

4/15/2015

Muscle Supplements and Testicular Cancer

A study of men who have used muscle-building supplements shows a disturbing increase in the risk of testicular cancer. More information is in the Muscle Enhancers (Creatine and Branched-chain Amino Acids) Review >>

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

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).

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

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

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 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

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

November 21, 2010

FDA Warns Consumers Not to Use Vigor-25

On November 19, 2010, the U.S.

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

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 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

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

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

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

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).

Recalls & Warnings

May 18, 2023

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

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

News Release

December 14, 2010

DHEA supplements, touted for anti-aging and strength, reviewed by ConsumerLab.com. Testing finds one brand with only 14.7% of labeled amount

WHITE PLAINS, NEW YORK — DECEMBER 14, 2010 — Recent tests of DHEA supplements showed that most products contained their claimed amounts of the controversial ingredient, but one provided only 14.7% of its listed amount, the testing company ConsumerLab.com reported today.

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

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

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

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

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.

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

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

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

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

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

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

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

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

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 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 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.

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 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

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

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

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

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

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

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

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.

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 ...

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

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.

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.

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.

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.

News Release

December 08, 2003

ConsumerLab.com dispels myths about HGH human growth hormone supplements sold widely on Internet

WHITE PLAINS, NY — December 8, 2003 — ConsumerLab.com has released a review of the scientific evidence behind human growth hormone (hGH or HGH) supplements.

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

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

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

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

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

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

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

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

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 ...

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.

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).

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.

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.

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

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 ...

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

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

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.

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

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

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

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

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

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

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

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

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

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

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

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

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.

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

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

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.

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

April 16, 2014

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

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

Recalls & Warnings

February 13, 2013

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

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

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

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

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

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

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

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

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

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

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

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

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 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

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

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.

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

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

June 09, 2005

FTC Cracks Down on "HGH" Supplements; $20 Million in Consumer Redress

On June 9, 2005, The Federal Trade Commission (FTC) announced that two Florida businesses have agreed to a federal court order requiring them to pay up to $20 million in consumer redress – the largest monetary judgment ever obtained in an FTC health fraud case – to settle charges that they ...

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

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

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

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 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 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

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

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

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.

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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 03, 2011

FDA Warns: Beware of Bogus STD Products

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

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

October 29, 2016

Steroid "Alternatives" Not Permitted In Dietary Supplements, FDA Warns

On September 27, 2016, the FDA issued a warning letter to Proprietary Wellness, L.L.C.

Recalls & Warnings

May 23, 2016

Amino Acid Supplements Recalled

On May 18, 2016, Ultimate Nutrition Inc. issued a recall of its Amino Gold amino acid tablets and capsules because they contain undeclared milk in the form of hydrolyzed whey protein.

Recalls & Warnings

April 26, 2015

FDA Identifies More Products Listing Synthetic Amphetamine

On April 22, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called beta- methylphenylethylamine (BMPEA) on product labels.

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.

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.