Reported Aug 29, 2012 · Terminated

V Maxx Rx, All Natural Male Enhancement, a) 1-count blister pack UPC Code 2802803561; b) 5-count blister pack UPC Code…

The Menz Club, LLC

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: The Menz Club, LLC · 103 W. Washington Street · Ridgeland, MS · 39157

Is this the product you have?

4 of 4 products

Products covered by this recall
#Product as published
11-count blister pack UPC Code 2802803561
25-count blister pack UPC Code 0972859402
310-count bottle UPC code 0913251017 bottles, Manufactured by The Menz Club, LLC, 103
4Washington Street, Suite B5, Ridgeland, MS 39157, Phone: 601-866-6746
Lot codes and dates
    • Lot #s: a) 101108
    • 101009
    • 101010
    • 101011
    • b) 101108
    • 101109
    • 101110
    • c) 301000
    • 301001
Amount recalled
585,000 Capsules

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Marketed Without An Approved NDA/ANDA: Samples tested by FDA were found to contain sulfoaildenafil, an analogue of sildenafil, an FDA approved drug used in the treatment of male erectile dysfunction, making these products unapproved new drugs.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Dec 7, 2015 · Data as of Sep 19, 7:10 PM UTC

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