FDAFDA · Food and drugs·Recall number D-1614-2014
MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663
Published October 8, 2014 · Recall initiated: May 5, 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: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Eugene Oregon, Inc.
- Distributor
- To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC
- Lot
- All lots
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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