D-003-2013 Class II Terminated

Recalled by Caraco Pharmaceutical Laboratories Ltd. — Cranbury, NJ

Recall Details

Product Type
Drugs
Report Date
October 10, 2012
Initiation Date
August 21, 2012
Termination Date
November 19, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
a) 2424 Cartons b) 2675 Cartons

Product Description

Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose Capsules (5x6 blister cards per carton), NDC 57664-135-64, b) 100-count unit dose Capsules (25x4 blister cards per carton), NDC 57664-135-65, Distributed by: Caraco Pharmaceutical Laboratories, Ltd. Detroit, MI 48202 Affiliate of Sun Pharmaceutical Industries, Inc.

Reason for Recall

Crystallization: Presence of crystals of Nimodipine within the capsule solution.

Distribution Pattern

One direct account - Caraco Pharmaceutical Labroatories, LTD Detroit, Michigan 78 sub accounts

Code Information

Lot: a) 3305.039B, Exp 07/13; b) 3305.039A, Exp 07/13