Eugene Oregon, Inc. recalls MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663
Recalled October 8, 2014 · FDA recall D-1614-2014 · Eugene Oregon
Hazard
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil. · FDA Class I
Units
57 boxes
Sold at
To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC
Description
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Product
MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663
Manufacturer(s)
Eugene Oregon, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →