American Health Packaging oxycodone recalled for blister seal defects
American Health Packaging is recalling certain oxycodone hydrochloride 5 mg tablets because the blister card seals are defective or missing. This allows tablets to fall out of their compartments. The recall affects 31,676 packages distributed nationwide with specific lot numbers and expiration dates.
From the FDA notice · Read the official notice ↗ · All Amerisource recalls
What to do
- Check if you have oxycodone tablets from lot #1027932 (expires 06/30/2027) or lot #1028360 (expires 08/31/2027)
- Inspect the blister card seal for weakness or damage before use
- Contact your pharmacy or doctor if you have an affected package
- Do not use tablets that have fallen loose from their compartments
Is yours affected?
Compare your label or packaging with the recalled product.
- 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
- Sold in
- Nationwide
- Made for
- Adults (0 months and older)
Details
- Units affected
- 31,676 packages
- Illnesses reported
- None reported
- Manufactured in
- 2550 John Glenn Ave Ste A, N/A, Columbus, OH, United States
- Classification
- Class II
- Recall number
- D-0338-2026
In the FDA's words
- Description
- 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 Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities. Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027 Distribution: Nationwide in the USA Affected quantity: 31,676 packages
- Hazard
- Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.