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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted 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. The warning follows a recall of one lot of SANGTER Energy Supplement 3000 mg in August 2022 due to the presence of this drug.
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.
Recalled Sangter Natural Male Energy Supplement (see product images) is marketed as a dietary supplement for male sexual enhancement and was sold on various websites and possibly in some small retail stores. It is packaged in 7-count blister packs within a carton.
Consumers and healthcare providers can report any adverse reactions to the FDA’s MedWatch Voluntary Reporting Program.
See ConsumerLab’s Review of Sexual Enhancement Supplements for tests of related products.
For more information, use the link below.
Public Notification: Sangter Natural Male Energy Supplement Contains Hidden Drug Ingredient
See related recalls and warnings:
Sexual Enhancement Supplement Recalled Due to Sildenafil
FDA Warns Sellers of Tainted Honey-Based Sexual Enhancement Products
Honey-Based Enhancement Supplement Recalled
FDA Finds Unapproved Drugs in Many Weight Loss and Sexual Enhancement Products Sold Online
FDA Warns Consumers Not to Use Certain Sexual Enhancement Supplements
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
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.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
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