FDAFDA · Food and drugs·Recall number D-1338-2014
Magic For Men, packaged in 1ct blister pack and 12-pill/bottle, 390 mg Manufactured For: BTQ Ski, Inc., Chicago, IL 60638
Published May 28, 2014 · Recall initiated: January 9, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Schindele Enterprises dba Midwest Wholesale
- Distributor
- Distributed to PA, IL, TX, IA, GA, CT, FL, CA, LA, NY, MD, NV, and WI
- Lot
- 12-ct.bottle, Lot GP808, Exp. 10/16, 1-ct. blister Lot BN030613, EXP 020615
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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