Blue Male Enhancement Pill — Class I drug recall D-266-2013
Ongoing recall by The Menz Club, LLC, reported 2013-04-24, distributed in UT. Marketed without an Approved NDA/ANDA; product found to contain sulfoaildenafil, an analogue of sildenafil, th
| Recall number | D-266-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Menz Club, LLC, Ridgeland, MS, United States |
| Recall initiated | 2012-03-10 |
| Classified | 2013-04-18 |
| Reported by FDA | 2013-04-24 |
| Distributed | UT |
| Quantity | 50,000 capsules |
| Reason classes | unapproved product |
Product
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-266-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.