D-0183-2025 Class III Ongoing
FDA drug recall D-0183-2025 was initiated by West-Ward Columbus Inc on December 19, 2024 and is designated Class III. Reason for recall: Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only. The recall status is ongoing. Affected quantity: 2591 100-count boxes.
Recall Details
- Product Type
- Drugs
- Report Date
- January 15, 2025
- Initiation Date
- December 19, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2591 100-count boxes
Product Description
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.
Distribution Pattern
US Nationwide.
Code Information
Lot # AC2556A; Exp. 03/2027