# FDA recall D-1657-2012

> **The Menz Club, LLC** · Class I · drug recall initiated 2012-05-25.

## Product

V Maxx Rx, All Natural Male Enhancement, a) 1-count blister pack UPC Code 2802803561; b) 5-count blister pack UPC Code 0972859402; c) 10-count bottle UPC code 0913251017 bottles, Manufactured by The Menz Club, LLC, 103 W. Washington Street, Suite B5, Ridgeland, MS  39157, Phone: 601-866-6746

## Reason for recall

Marketed Without An Approved NDA/ANDA: Samples tested by FDA were found to contain sulfoaildenafil, an analogue of sildenafil, an FDA approved drug used in the treatment of male erectile dysfunction, making these products unapproved new drugs.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1657-2012
- **Recalling firm:** The Menz Club, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-05-25
- **Report date:** 2012-08-29
- **Termination date:** 2015-12-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ridgeland, MS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1657-2012

## Citation

> AI Analytics. FDA recall D-1657-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1657-2012. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*