D-003-2013 Class II Terminated
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