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 Sun Pharmaceutical Industries Inc. Due to Crystallization; crystallized nimodipine
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 Sun Pharmaceutical Industries Inc. 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: 46387 Cartons
Why Was This Recalled?
Crystallization; crystallized nimodipine
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sun Pharmaceutical Industries Inc.
Sun Pharmaceutical Industries Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report