FDA Drug recall D-1657-2012
V Maxx Rx, All Natural Male Enhancement, a) 1-count blister pack UPC Code 2802803561
- FDA Drug
- Class I
- terminated
- Published 2012-08-29
On 2012-08-29 the FDA classified a Class I recall of V Maxx Rx, All Natural Male Enhancement, a) 1-count blister pack UPC Code 2802803561 by The Menz Club, citing 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 e….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1657-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-05-25 |
| Published | 2012-08-29 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | The Menz Club |
| Distribution | US |
Product
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
Reason
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.
Identifiers
| code_info | Lot #s: a) 101108, 101009, 101010, 101011; b) 101108, 101109, 101110; c) 301000, 301001 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1657-2012%22
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