Recalls and Warnings

Sexual Enhancement Supplements Containing Prescription Drugs Recalled

 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.
(Date Posted: 9/21/2017)

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

  • Papa Zen 3300 capsules, Lot# NSS050888

  • Fifty Shades 6000 capsules, All Lots

  • Grande X 5800 capsules, All Lots
Sildenafil and tadalafil, the active ingredients in the prescription drugs Viagra and Cialis, respectively, are prescribed for erectile dysfunction. These drugs 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 products were packaged in 1-count blister cards and distributed throughout the country via online sales.

Consumers who have purchased these supplements should discontinue use immediately and contact their healthcare provider if they have experienced any adverse side effects. Consumers and healthcare providers are also encouraged to report any adverse reactions to the FDA's MedWatch Adverse Event Reporting Program.

See related recalls and warnings:

Hidden Drugs Found in Sexual Enhancement Products

Herbal "Sexual Enhancement Coffee" Recalled

Herbal "Sexual Enhancement Coffee" Recalled, One Death Reported

FDA Finds Hidden Drug Ingredients in Sexual Enhancement Supplements

Sexual Enhancement Supplements for Men and Women Recalled

To read the complete recall, use the link below.

https://www.fda.gov/Safety/Recalls/ucm576785.htm



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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