Posted September 12, 2010

Mr. Magic Male Enhancer Recalled

The U.S. FDA posted a recall announcement daated August 18, 2010 from Glow Industries regarding "Mr. Magic Male Enhancer from Don Wands." The product was found by the company to contain Hydroxythiohomosildenafil and Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making Mr. Magic Male Enhancer an unapproved new drug. These active ingredients are not listed on the product label. Product manufactured containing lot numbers 9041401, 251209 and 8121904 are included in this recall.

The recall is being conducted as a precautionary measure. No illnesses or adverse effects have been reported to the company to date in connection with the product.

The undeclared ingredients may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with conditions, and consumers may seek types of products to enhance sexual performance.

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