FDA Drug recall D-266-2013
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
- FDA Drug
- Class I
- ongoing
- Published 2013-04-24
On 2013-04-24 the FDA classified a Class I recall of Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS by The Menz Club, citing marketed without an Approved NDA/ANDA; product found to contain sulfoaildenafil, an analogue of sildenafil, the active ingredient in a FDA approved product used for erectile dysfu….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-266-2013 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2012-03-10 |
| Published | 2013-04-24 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | The Menz Club |
| Distribution | UT |
Product
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
Reason
Marketed without an Approved NDA/ANDA; product found to contain sulfoaildenafil, an analogue of sildenafil, the active ingredient in a FDA approved product used for erectile dysfunction, making it an unapproved new drug
Identifiers
| code_info | None |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-266-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.