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
Take action
Contact the company
📍Recalling firmThe Menz Club, LLC103 W. Washington Street, Suite B5 · Ridgeland, MS 39157
✎ GovInfoNow plain-language explainer
The Menz Club, LLC has recalled its Blue Male Enhancement Pill, a bulk product distributed in Utah. The recall is necessary because the pills were marketed without an approved New Drug Application and were found to contain sulfoaildenafil, an unapproved analogue of sildenafil. This makes the product an unapproved new drug rather than a safe supplement. Read more at govinfonow.com/recall/48944-the-menz-club-llc-recalls-blue-male-enhancement-pill-bulk.
“The Menz Club Recalls Blue Male Enhancement Pills Due to Unapproved Drug.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/48944-the-menz-club-llc-recalls-blue-male-enhancement-pill-bulk. Based on FDA recall #D-266-2013 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-266-2013%22&limit=1).
The Food and Drug Administration announced on March 10, 2012, that The Menz Club, LLC is recalling Blue Male Enhancement Pill bulk product. The agency stated the drug was marketed without an approved New Drug Application or Abbreviated New Drug Application.
How to tell if you have it
Brand: The Menz Club
Product: Blue Male Enhancement Pill
Quantity: 50,000 capsules
Distribution: Utah
The hazard
The FDA said the product was found to contain sulfoaildenafil, an analogue of sildenafil. Sildenafil is the active ingredient in an FDA-approved drug used for erectile dysfunction, making the recalled item an unapproved new drug.
Context
GovInfoNow's records show The Menz Club, LLC has one other recall on record since May 25, 2012. On May 25, 2012, the company issued a recall for V Maxx Rx due to an unapproved drug containing sulfoaildenafil. Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (December 15, 2025), SUN PHARMACEUTICAL Xyvona 3mg Tablets Recall (May 22, 2026), and SILINTAN 25-pill bottle recalled for undeclared meloxicam in FDA analysis (October 20, 2025).
How to tell if you have this one
Look for Blue Male Enhancement Pill produced by The Menz Club, LLC of Ridgeland, MS. The recalled items are bulk products distributed in Utah, with a total quantity of 50,000 capsules.
Brand
The Menz Club
Category
Drug
Based on the official FDA remedy
What to do — step by step
Stop using the product
Do not consume the Blue Male Enhancement Pill as it contains an unapproved drug ingredient.
Dispose of the pills
Discard any remaining bulk product to prevent accidental ingestion.
Where it went and when
Where it was distributed
Distributed in Utah.
Listed by the agency
Not listed
FDA distribution: “Utah” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Utah.
Recall timeline
FDA published this recall 13 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #D-266-2013 (March 10, 2012) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-266-2013 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 13, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.