# FDA recall D-1508-2020

> **Lannett Company, Inc.** · Class II · drug recall initiated 2020-08-10.

## Product

Prednisone Tablets, USP 2.5 mg, 100 tablets, Rx only,  Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, Manufactured by: Tianjin Tianyao Pharmaceuticals Co., Ltd No. 221 Huanghai Road, Tianjin Economical-Technological Development Area, Tianjin, China 300457  NDC 0527-2931-37

## Reason for recall

Labeling: Label Mix Up: bottle labeled to contain  Prednisone Tablets, USP 2.5 mg actually contained Prednisone Tablets, USP 10 mg

## Distribution

US Nationwide

## Key facts

- **Recall number:** D-1508-2020
- **Recalling firm:** Lannett Company, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2020-08-10
- **Report date:** 2020-08-26
- **Termination date:** 2022-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Philadelphia, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1508-2020

## Citation

> AI Analytics. FDA recall D-1508-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-1508-2020. Source: US FDA. Licensed CC0.

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