Could cause temporary or reversible harm; serious harm is unlikely.
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
| Brand name | OXYCODONE HYDROCHLORIDE |
| Generic name | OXYCODONE HYDROCHLORIDE |
| Active ingredient(s) | OXYCODONE HYDROCHLORIDE |
| Distributed by / for | American Health Packaging, Columbus, Ohio 43217, Carton |
| NDC | 10702-018 |
| Full product label | 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 |
| Distribution | Nationwide in the USA |
| Quantity | 31,676 packages |
| Recall initiated | 2026-01-14 |
| Report date | 2026-02-18 |
| Recall completed | — |
| Recall number | D-0338-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Columbus OH United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗