Recalls and Warnings

Men's Enhancement 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: 12/21/2019)

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.

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 2, 4, and 10 capsule blister pack cards and were sold locally to 2 Dallas convenience stores.

Consumers who have purchased these products in October, 2019 should stop consuming them and return any unused product to Motto International Corp. 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:

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

Sexual Enhancement Supplement for Men Recalled

For more information, use the link below.

Motto International Corp. Issues Voluntary Recall of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000, 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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