May 29, 2012
The Menz Club, LLC Recalls V Maxx Rx
The Missouri Department of Health and Senior Services received the following news release regarding the recall of V Maxx RX due to Undeclared Sulfoaildenafil. 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.
The following lot numbers have been recalled:
Single Count, UPC Code 2802803561, Lot Nos. 101108, 101009, 101010, 101011 , Five Count, UPC Code 0972859402, Lot Nos.: 101108, 101109, 101110, Ten Count, UPC code 0913251017, Lot Nos.: 301000, 301001
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.
The affected products may have been ordered online at www.vmaxxrx.com or www.themenzclub.net and were distributed to customers and distributors nationwide. This product is marketed as a dietary supplement intended for use as a male enhancement product and is packaged in one (1) and five (5) count blister packs and ten (10) count bottles.
The full recall can be found at www.fda.gov/Safety/Recalls/ucm305795.htm?source=govdelivery.