Key Takeaway
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS by The Menz Club, LLC was recalled on March 10, 2012. The hazard: Marketed without an Approved NDA/ANDA; product found to contain sulfoaildenafil, an analogue of sildenafil, the active ingredient in a FDA approved pr...
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
Description
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
Hazard / 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
Class I: Dangerous or defective product that could cause serious health problems or death.
Class I is the most serious recall classification used by the FDA, indicating a reasonable probability of serious health consequences or death.
Products Affected
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
DrugsCompany Information
The Menz Club, LLC
Ridgeland, MS, United States
View all 2 recalls by The Menz Club, LLC →Distribution
Utah
Related Recalls
Frequently Asked Questions
Is this recall still active?
Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.
How do I check if my product is affected?
Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.
What remedy is available for this recall?
Check the remedy section above or contact the manufacturer directly for current remedy options.
Where can I find the original recall notice?
This recall was issued by FDA Drug. Visit the agency's official website for the original notice.