Oxycodone Hydrochloride Tablets 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 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
Why was Oxycodone Hydrochloride Tablets recalled?
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027
- 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
- Recalling firm
- Amerisource Health Services LLC
- Quantity
- 31,676 packages
- Distribution
- Nationwide in the USA
- Recall date
- February 18, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)