# FDA recall D-0026-2022

> **Dr. Reddy's Laboratories, Inc.** · Class II · drug recall initiated 2021-10-05.

## Product

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

## Reason for recall

CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0026-2022
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-10-05
- **Report date:** 2021-10-27
- **Termination date:** 2022-12-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0026-2022

## Citation

> AI Analytics. FDA recall D-0026-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0026-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*