# FDA recall D-0599-2021

> **Dr. Reddy's Laboratories, Inc.** · Class III · drug recall initiated 2021-05-04.

## Product

Atorvastatin Calcium Tablets, USP 10 mg*, Rx Only, 500 count bottle, Mfd By: Dr. Reddy's Laboratories Limited, Bachupally 500 090, India,  NDC 55111-121-05.

## Reason for recall

Failed Impurities -Degradation Specifications:due to presence of ATV cyclo IP and FP impurities

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0599-2021
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-05-04
- **Report date:** 2021-06-02
- **Termination date:** 2023-02-16

- **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-0599-2021

## Citation

> AI Analytics. FDA recall D-0599-2021. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/D-0599-2021. Source: US FDA. Licensed CC0.

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