The Menz Club, LLC Issues a Voluntary Nationwide Recall of V Maxx Rx due to Undeclared Sulfoaildenaf
date:May 28, 2012
e related to taking or using these products.


Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.


Online: https://www.accessdata.fda.gov/scripts/medwatch/medwatch-online.htm
Regular mail: use postage-paid, pre-addressed Form FDA 3500 available at:


http://www.fda.gov/Safety/MedWatch/HowToReport/DownloadForms/default.htm. Mail to address on the pre-address

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