Print Page

Products found to contain undeclared medicines

The United States: The Menz Club, LLC Issues a Voluntary Nationwide Recall of V Maxx Rx due to Undeclared Sulfoaildenafil
The Menz Club, LLC is conducting a voluntary recall of V Maxx Rx to the consumer level. FDA laboratory analysis of V Maxx Rx was found to contain undeclared sulfoaidenafil. Sulfoaidenafil is an analog of sildenafil, an FDA approved prescription drug used to treat Erectile Dysfunction (ED), making V Maxx Rx, an unapproved new drug. FDA advises that this poses a threat to consumers because sildenafil may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Men with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. This product is marketed as a dietary supplement intended for use as a male enhancement product. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using these products.

Please refer to the following website in FDA for details:

In Hong Kong, the above product is a not a registered pharmaceutical product. Related news has been released by the FDA and was posted on the website of Drug Office on 17 May 2012.

Ends/ Monday, May 28, 2012
Issued at HKT 12:00
Related Information:
The United Kingdom: Advice to consumers not to use ten herbal products used to t... Posted 2012-11-28
Canada: Foreign Product Alert: VMaxx Rx Posted 2012-08-02
The United States: Public Notification: "VMaxx Rx" Contains Hidden Drug Ingredie... Posted 2012-05-17