US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 22, 2018 (9 years ago)

Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for…

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

Why it was recalled

Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol

What was recalled

Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY --- NDC 31722-917-01

Recalling firm
Ascent Pharmaceuticals, Inc.
NDC code
31722-917-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0248-2018

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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