D-1415-2014 Class II Terminated
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.