West-Ward Columbus Inc: Drug Recall

Recall #D-0183-2025 · 12/19/2024

Class III: Low Risk

Recall Details

Recall Number: D-0183-2025
Classification: Class III
Product Type: Drug
Recalling Firm: West-Ward Columbus Inc
Status: Ongoing
Date Initiated: 12/19/2024
Location: Columbus, OH, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 2591 100-count boxes

Reason for Recall

Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.

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

Distribution Pattern

US Nationwide.

Other Recalls by West-Ward Columbus Inc

Class III: Low Risk 09/22/2023

Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.

View all recalls by West-Ward Columbus Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.