FDA Drug · D-0338-2026

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11

Class II · Ongoing

Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.

Affected lots / codes — check yours against thisLots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027

Recalling firm: Amerisource Health Services LLC, Columbus, OH
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 31,676 packages
Distribution: Nationwide in the USA
Recall initiated: January 14, 2026
Classified: February 13, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0338-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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