US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 21, 2012 (14 years ago)

Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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.

Recalling firm
Caraco Pharmaceutical Laboratories Ltd.
NDC code
57664-135-64
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-003-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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