Home / Recalls / Eugene Oregon, Inc. / D-1614-2014

D-1614-2014 Class I Terminated

Recalled by Eugene Oregon, Inc. — Levittown, PA

Recall Details

Product Type: Drugs
Report Date: October 8, 2014
Initiation Date: May 5, 2014
Termination Date: April 1, 2015
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 57 boxes

Product Description

MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663

Reason for Recall

Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.

Distribution Pattern

To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC

Code Information

All lots