US Drug Recall Register
Class I · High risk Ongoing Initiated Mar 10, 2012 (14 years ago)

Blue Male Enhancement Pill

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS

Recalling firm
The Menz Club, LLC
Origin
MS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-266-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.