Class III
Ongoing
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.
This recall is currently active, issued July 27, 2022. It was issued by Glenmark Pharmaceuticals Inc., Usa.
- Recall Initiated
- June 29, 2022
- Posted
- July 27, 2022
- Recall Number
- D-1282-2022
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 168936 bottles
- Firm Location
- Mahwah, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Tablet/Capsule Specification : Capsule breakage
Distribution
USA Nationwide
Lot / Code Info
Lot#: 17201639, Exp 08/2022; 17201759, Exp 09/2022; 17202067, Exp 10/2022; 17210696, Exp 02/2023; 17210092, Exp 11/2022; 17210145, Exp 12/2022; 17210732, Exp 02/2023; 17211062, Exp 04/2023; 17211441, Exp 05/2023; 17211670, Exp 06/2023; 17211810, Exp 07/2023; 17211862, 17212020, 17212068, Exp 08/2023; 17212438, Exp 10/2023; 17220172, 17220251, Exp 12/2023.
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