PredniSONE Tablets USP — Class II drug recall D-0008-2017
Terminated recall by West-Ward Pharmaceutical, reported 2016-10-12, distributed nationwide. Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.
| Recall number | D-0008-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | West-Ward Pharmaceutical, Columbus, OH, United States |
| Recall initiated | 2016-10-03 |
| Classified | 2016-10-06 |
| Reported by FDA | 2016-10-12 |
| Terminated | 2017-12-18 |
| Distributed | Nationwide (US) |
| Quantity | 15,109 bottles |
| NDC | 00054-0017, 00054-0017-20, 00054-0017-25, 00054-0017-29, 00054-0018, 00054-0018-20, 00054-0018-25, 00054-0018-29, 00054-0019, 00054-0019-20, 00054-0019-25, 00054-3721, 00054-3721-44, 00054-3722, 00054-3722-50, 00054-3722-63, 00054-4728, 00054-4728-25, 00054-4728-31, 00054-4741, 00054-4741-25, 00054-4741-31, 00054-4742, 00054-4742-25, 00054-8724 and 5 more |
| Lot numbers | 660621A |
| Expiration dates | 2018-01-31 |
Product
PredniSONE Tablets USP, 1 mg, 100-count bottles, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-4741-25.
Reason for recall
Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.
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-0008-2017. 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.