Reported Jul 23, 2025 · Ongoing
Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle, Rx Only, Manufactured by: Dr. Reddy's Laboratories…
Dr. Reddy's Laboratories, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Dr. Reddy's Laboratories, Inc. · 107 College Rd E · Princeton, NJ · 08540-6623
Is this the product you have?
- Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle, Rx Only
- Manufactured byDr. Reddy's Laboratories Limited, Bachupally - 500 090 INDIA
- Manufactured forQualient Pharmaceuticals Health LLC, Grand Cayman, Cayman Islands, NDC 82009-022-10. NDC 82009-022-10
- Lot codes and dates
- Lot
C2403017Exp 12/31/2026
- Lot
- Amount recalled
- 1476 bottles
Where it was sold
- Nationwide
Why it was recalled
Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
This product could cause temporary or reversible health problems — stop using it.
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