US Drug Recall Register
Class III · Low risk Ongoing Initiated Dec 19, 2024 (2 years ago)

Methadone Hydrochloride Tablets, USP, 5mg, 10x10 Unit-Dose Tablets, Rx Only, Distributed…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

What was recalled

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

Recalling firm
West-Ward Columbus Inc
NDC code
0054-0709-20
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0183-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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