Prednisone Tablets — Class II drug recall D-1508-2020
Terminated recall by Lannett Company, Inc., reported 2020-08-26, distributed nationwide. Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP 2.5 mg actually contained Prednisone
| Recall number | D-1508-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lannett Company, Inc., Philadelphia, PA, United States |
| Recall initiated | 2020-08-10 |
| Classified | 2020-08-17 |
| Reported by FDA | 2020-08-26 |
| Terminated | 2022-07-22 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| NDC | 00527-2931-37 |
| Lot numbers | PE190701E1 |
| Expiration dates | 2021-06-20 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1508-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.