Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Aspirin and Extended-Release Dipyridamole Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to Failed Tablet/Capsule Specification : Capsule breakage
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 Glenmark Pharmaceuticals Inc., USA directly.
Affected Products
Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-405-60.
Quantity: 168936 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specification : Capsule breakage
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Glenmark Pharmaceuticals Inc., USA
Glenmark Pharmaceuticals Inc., USA has 139 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report