# FDA recall D-0583-2024

> **Dr. Reddy's Laboratories, Inc.** · Class II · drug recall initiated 2024-06-07.

## Product

Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.

## Reason for recall

Presence of foreign substance.

## Distribution

IL, MS, OH

## Key facts

- **Recall number:** D-0583-2024
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-06-07
- **Report date:** 2024-07-10
- **Termination date:** 2025-12-22

- **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-0583-2024

## Citation

> AI Analytics. FDA recall D-0583-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-0583-2024. Source: US FDA. Licensed CC0.

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