US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 29, 2021 (5 years ago)

Oxycodone Hydrochloride Tablets, USP C-II, 5 mg, 100 count bottles, Rx Only, Manufactured…

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

Why it was recalled

Out-of-specification impurity test result observed at 18-month long term stability time point.

What was recalled

Oxycodone Hydrochloride Tablets, USP C-II, 5 mg, 100 count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202. Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873. NDC 43386-432-01

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
43386-432-01
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0358-2022

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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