Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Omeprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to CGMP Deviations: Customer complaint for the presence of...
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 Dr. Reddy's Laboratories, Inc. directly.
Affected Products
Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle within a carton, Distributed by Cardinal Health, Dublin, OH 43017, NDC 70000-0232-1
Quantity: 8,976 bottles
Why Was This Recalled?
CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Dr. Reddy's Laboratories, Inc.
Dr. Reddy's Laboratories, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report