US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jan 14, 2026 (8 months ago)

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Amerisource Health Services LLC
NDC code
68084-354-01
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0338-2026

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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