Recalls / Active ingredient / Omeprazole
Omeprazole
3 FDA drug recalls involving the active ingredient “Omeprazole”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-06-30 | Class II | Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle, Rx Only, Manufactured by: Dr. Reddy's Labor | Dr. Reddy's Laboratories, Inc. |
| 2024-02-02 | Class II | Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1,680mg, This packet contains 40mg of omeprazole a | Bausch Health Companies, Inc. |
| 2013-09-16 | Class II | Omeprazole Delayed-Release Capsules, USP, 20 mg, Rx Only, 1000 Capsules per bottle, Distributed by: Kremers Ur | Kremers Urban Pharmaceuticals, Inc. |