Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nimodipine Capsules 30 mg Recalled by Caraco Pharmaceutical Laboratories Ltd. Due to Crystallization: Presence of crystals of Nimodipine within the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Caraco Pharmaceutical Laboratories Ltd. directly.
Affected Products
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.
Quantity: a) 2424 Cartons b) 2675 Cartons
Why Was This Recalled?
Crystallization: Presence of crystals of Nimodipine within the capsule solution.
Where Was This Sold?
One direct account - Caraco Pharmaceutical Labroatories, LTD Detroit, Michigan 78 sub accounts
About Caraco Pharmaceutical Laboratories Ltd.
Caraco Pharmaceutical Laboratories Ltd. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report