# FDA recall D-0312-2024

> **Dr. Reddy's Laboratories, Inc.** · Class III · drug recall initiated 2024-01-18.

## Product

Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01

## Reason for recall

Misprint on tablet

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0312-2024
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-01-18
- **Report date:** 2024-02-14

- **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-0312-2024

## Citation

> AI Analytics. FDA recall D-0312-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/D-0312-2024. Source: US FDA. Licensed CC0.

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