Recalls and Warnings

"Active Male" Supplement Recalled

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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.
(Date Posted: 3/17/2020)

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.

Tadalafil, the active ingredient in Cialis, 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.

The recalled supplements are packaged in small foldable cardboard with the image of a Trojan helmet and were sold in the Natural Remedy Store in San Antonio, TX, and online through NaturalRemedyStore.com.

Consumers who have purchased these products should stop consuming them and return any unused product to Natural Remedy Store. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Consumers and healthcare providers can report any adverse reactions to the FDA's MedWatch Voluntary Reporting Program.

(See ConsumerLab.com's Review of Sexual Enhancement Supplements for tests of related products.)

See related warnings:

Men's Enhancement Supplement Recalled

Silver Bullet Supplement for Men Recalled

Libido Supplement for Men and Women Recalled

Green Lumber Enhancement Supplements Recalled

Liquid Vitamin C for Men Recalled

Titanium 4000 Capsules for Men Recalled

"The Beast" Supplement for Men Recalled

For more information, use the link below.

Natural Remedy Store Issues Voluntary Worldwide - Recall of Active Male Due to Presence of Undeclared Tadalafil



For other Recalls and Warnings click HERE.
For information about reporting serious reactions and problems with medical products to the U.S. Food and Drug Administration through its MedWatch reporting program, please go to http://www.fda.gov/medwatch/how.htm.


 

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