CLASS I ONGOING Drug recall · Reported 24 Apr 2013 · FDA Enforcement Report
Blue Male Enhancement Pill, bulk product, by The Menz Club recalled
The Menz Club is recalling Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS, distributed in Utah. The recall was initiated on 10 Mar 2012 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-266-2013
- FDA event ID
- 63684
- Recalling firm
- The Menz Club, Ridgeland, MS
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 10 Mar 2012
- FDA classified
- 18 Apr 2013
- Reported
- 24 Apr 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Hidden Drug Ingredients
Timeline
| 10 Mar 2012 | Recall initiated by company | |
| 18 Apr 2013 | Classified by FDA | +404 days |
| 24 Apr 2013 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
Where it was distributed
Utah
Questions about this recall
Is Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS recalled?
Yes. The Menz Club recalled Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS on 10 Mar 2012. The recall is Class I and its status is Ongoing. Recall number D-266-2013.
Why was it 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
Which lots are affected?
None
Where was it sold?
Utah
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from The Menz Club
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | V Maxx Rx, All Natural Male Enhancement, a) recalled by The Menz Club | The Menz Club | Hidden Drug Ingredients | Nationwide |