FDAClass IApril 24, 2013

Blue Male Enhancement Pill recall

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

Why was Blue Male Enhancement Pill 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 should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

None

Product
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
Recalling firm
The Menz Club, LLC
Quantity
50,000 capsules
Distribution
Utah
Recall date
April 24, 2013
Classification
Class I
Status
Ongoing
Agency
FDA (drug)
Open FDA enforcement record Latest recalls