D-1415-2014 Class II Terminated

Recalled by Caraco Pharmaceutical Laboratories, Ltd. — Detroit, MI

Recall Details

Product Type
Drugs
Report Date
July 9, 2014
Initiation Date
June 12, 2014
Termination Date
May 6, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
26,530 30-Count Bottles; 14,597 90-Count Bottles

Product Description

Venlafaxine Hydrochloride Extended-Release Tablets, 150 mg, Rx only, Packaged in 30 Count and 90 Count Bottles. Distributed by: Caraco Pharmaceutical Laboratories, Ltd., 1150 Elijah McCoy Drive, Detroit, MI 48202; Manufactured at: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India. 30-Count Bottle NDC: 41616-758-83, 90-Count Bottle: NDC 41616-758-81.

Reason for Recall

Failed Dissolution Specifications: Stability results found the product did not meet the drug dissolution specifications.

Distribution Pattern

Nationwide including Puerto Rico

Code Information

30 Count Bottle: Lot #: JKL5054A, Expiry: 08/2014; Lot #: JKM2305A, Expiry: 03/2015. 90 Count Bottle: Lot #: JKL5054B, Expiry: 08/2014; Lot #: JKM2305B, Expiry: 03/2015.