United StatesOxycodone Hydrochloride Tablets, USP (CII) 5 mg, 100-count (10 x 10) blister cards per carton (Carton NDC 68084-354-01; Blister NDC 68084-354-11) from NDC 10702-018 (KVK‑Tech Inc.), distributed by American Health Packaging, lots 1027932 (exp. 06/30/2027) and 1028360 (exp. 08/31/2027), are being recalled by Amerisource Health Services LLC. The recall is due to defective card seal defects (weak or non-existent seals) that can allow tablets to fall out of their cavities; it is ongoing and covers 31,676 packages distributed nationwide in the USA.
What's being 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, Columbus, OH, United States.
How to identify it
Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027
The hazard
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Nationwide in the USA
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)