Paroxetine Tablets — Class II drug recall D-0091-2018
Terminated recall by Amerisource Health Services, reported 2017-11-29, distributed nationwide. Presence of Foreign Tablets/Capsules.
| Recall number | D-0091-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Amerisource Health Services, Columbus, OH, United States |
| Recall initiated | 2017-10-24 |
| Classified | 2017-11-21 |
| Reported by FDA | 2017-11-29 |
| Terminated | 2018-06-19 |
| Distributed | Nationwide (US) |
| NDC | 68084-0044, 68084-0044-01, 68084-0044-11, 68084-0044-65, 68084-0045, 68084-0045-01, 68084-0045-11, 68084-0046, 68084-0046-01, 68084-0046-11, 68084-0047, 68084-0047-01, 68084-0047-11 |
| Lot numbers | 172291 |
Product
Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Columbus, Ohio 43217, NDC 68084-046-01
Reason for recall
Presence of Foreign Tablets/Capsules.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0091-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.