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Medium risk Drugs & MedicationsClass II

Oxycodone Hydrochloride 5 mg Recall

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this

Updated January 14, 2026

Oxycodone Hydrochloride 5 mg tablets in 100-count blister cards are being recalled because defective container seals allow tablets to fall out of their cavities. This could lead to incorrect dosing or accidental exposure.

Is the Amerisource Health Services LLC recalled? Yes. This product was recalled by FDA on January 14, 2026. Details below.

What is recalled

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-count (10 x 10 blister cards per carton), NDC # 10702-018 (KVK-Tech Inc.), Carton NDC 68084-354-01, Blister NDC 68084-354-11. Distributed by American Health Packaging, Columbus, Ohio 43217.

Am I affected

You're affected if you have a prescription for Oxycodone Hydrochloride 5 mg tablets in a 100-count blister pack with the NDC numbers 68084-354-01 (carton) or 68084-354-11 (blister). Check the label on your medication bottle or blister card.

What to do right now

Stop using these tablets and contact your pharmacy or healthcare provider immediately. Do not use any tablets that have fallen out of their cavities or are loose in the package. Return the affected medication to your pharmacy for a replacement.

The hazard

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

Brands affected

Amerisource Health Services LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0338-2026
Classification
Class II
Recalled
January 14, 2026
Read the official notice

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