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
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
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send The Menz Club, LLC to request your refund or repair — edit it as you like.
Subject: Recall D-266-2013 — The Menz Club, LLC The Menz Club, LLC recalls Blue Male Enhancement Pill, bulk product, by The Menz Hello, I own a The Menz Club, LLC recalls Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS that is covered by recall D-266-2013 from The Menz Club, LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
