D-150-2013 Class II Terminated

Recalled by West-ward Pharmaceutical Corp. — Eatontown, NJ

FDA drug recall D-150-2013 was initiated by West-ward Pharmaceutical Corp. on December 7, 2012 and is designated Class II. Reason for recall: Presence of Foreign Substance: Uncharacteristic blacks spots on tablets. The recall status is terminated (terminated December 18, 2014). Affected quantity: 8,585 bottles.

Recall Details

Product Type
Drugs
Report Date
February 13, 2013
Initiation Date
December 7, 2012
Termination Date
December 18, 2014
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
8,585 bottles

Product Description

Carisoprodol Tablets, USP, 350 mg, packaged in a) 500-count tablets per bottle (NDC 0143-1176-05) and b) 1000-count tablets per bottle (NDC 0143-1176-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.

Reason for Recall

Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.

Distribution Pattern

Nationwide

Code Information

Lot #: 69364A, 69365A, and 69365B, Exp 10/15