Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
V Maxx Rx Recalled by The Menz Club, LLC Due to Marketed Without An Approved NDA/ANDA: Samples tested by...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact The Menz Club, LLC directly.
Affected Products
V Maxx Rx, All Natural Male Enhancement, a) 1-count blister pack UPC Code 2802803561; b) 5-count blister pack UPC Code 0972859402; c) 10-count bottle UPC code 0913251017 bottles, Manufactured by The Menz Club, LLC, 103 W. Washington Street, Suite B5, Ridgeland, MS 39157, Phone: 601-866-6746
Quantity: 585,000 Capsules
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About The Menz Club, LLC
The Menz Club, LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report