Drug recall D-0338-2026
Product
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
Reason for recall
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Lots and codes
Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027
Recall details
- Recalling firm
- Amerisource Health Services LLC, Columbus, OH
- Quantity
- 31,676 packages
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 14, 2026
Related products
- Oxycodone Hydrochloride – drug information
- NDC 68084-968 Oxycodone Hydrochloride · Oxycodone Hydrochloride 10 mg/1 · American Health Packaging
- NDC 68084-975 Oxycodone Hydrochloride · Oxycodone Hydrochloride 15 mg/1 · American Health Packaging
- NDC 10702-018 Oxycodone Hydrochloride · Oxycodone Hydrochloride 5 mg/1 · KVK-TECH,INC
- NDC 68084-983 Oxycodone Hydrochloride · Oxycodone Hydrochloride 30 mg/1 · American Health Packaging
- NDC 68084-354 Oxycodone Hydrochloride · Oxycodone Hydrochloride 5 mg/1 · American Health Packaging