D-0837-2016 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- May 11, 2016
- Initiation Date
- March 25, 2016
- Termination Date
- August 29, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21 bottles (910 extended release tablets)
Product Description
Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6), Rx Only, Manufactured by Teva Pharmaceuticals USA, Inc. Packaged by Bryant Ranch.
Reason for Recall
Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formulation.
Distribution Pattern
Nationwide
Code Information
Lot # 94983; Exp 10/17