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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted 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.
Sildenafil (the active ingredient in Viagra) is prescribed for erectile dysfunction. This drug can cause symptoms like headache and flushing and can interact with medications containing nitrates such as nitroglycerine, resulting in dangerously low blood pressure.
BIG GUYS Male Energy Supplement is marketed as an energy booster and sold on Amazon.com and in some retail stores.
Consumers and healthcare providers can report any adverse reactions to the FDA’s MedWatch Voluntary Reporting Program.
For more information about related products, see ConsumerLab’s answer to Which supplements help to improve energy and decrease fatigue?
Also see ConsumerLab’s Review of Sexual Enhancement Supplements.
For more information, use the link below.
BIG GUYS Male Energy Supplement contains hidden drug ingredient
See related recalls and warnings:
Gadget Island, Inc. Male Enhancement Supplements Found to Contain Prescription Drugs
PrimeZEN Enhancement Supplement for Men Found to Contain Prescription Drug
Male Sexual Enhancement Supplement Adam’s Secret Found to Contain Prescription Medication
Male Sexual Enhancement Supplement Found to Contain Prescription Drug
FDA Warns Consumers Not to Use Male Enhancement Supplement
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If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
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Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
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