# FDA recall D-0738-2022

> **Dr. Reddy's Laboratories, Inc.** · Class II · drug recall initiated 2022-03-23.

## Product

Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India, NDC 55111-399-90.

## Reason for recall

Failed Dissolution Specifications; during long term stability testing.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0738-2022
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-03-23
- **Report date:** 2022-04-06
- **Termination date:** 2024-02-02

- **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-0738-2022

## Citation

> AI Analytics. FDA recall D-0738-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-0738-2022. Source: US FDA. Licensed CC0.

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