Methadone Hydrochloride Tablets — Class III drug recall D-0183-2025
Ongoing recall by West-Ward Columbus Inc, reported 2025-01-15, distributed nationwide. Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
| Recall number | D-0183-2025 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | West-Ward Columbus Inc, Columbus, OH, United States |
| Recall initiated | 2024-12-19 |
| Classified | 2025-01-03 |
| Reported by FDA | 2025-01-15 |
| Distributed | Nationwide (US) |
| NDC | 00054-0709, 00054-0709-20, 00054-0709-25, 00054-0710, 00054-0710-20, 00054-0710-25 |
| Lot numbers | AC2556A |
| Expiration dates | 2027-03 |
Product
Methadone Hydrochloride Tablets, USP, 5mg, 10x10 Unit-Dose Tablets, Rx Only, Distributed by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922, NDC 0054-0709-20
Reason for recall
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
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-0183-2025. 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.