Aripiprazole Tablets — Class II drug recall D-0595-2018
Terminated recall by AMERICAN HEALTH PACKAGING, reported 2018-02-21, distributed nationwide. CGMP Deviations: lot made with active pharmaceutical ingredient that did not meet all its intended specificati
| Recall number | D-0595-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AMERICAN HEALTH PACKAGING, Columbus, OH, United States |
| Recall initiated | 2018-01-19 |
| Classified | 2018-03-13 |
| Reported by FDA | 2018-02-21 |
| Terminated | 2019-03-14 |
| Distributed | Nationwide (US) |
| Quantity | 270 cartons |
| Reason classes | cgmp |
| NDC | 60687-0157, 60687-0157-11, 60687-0157-21, 60687-0157-94, 60687-0168, 60687-0168-01, 60687-0168-11, 60687-0168-65, 60687-0179, 60687-0179-01, 60687-0179-11, 60687-0179-65, 60687-0191, 60687-0191-11, 60687-0191-21, 60687-0191-94, 60687-0202, 60687-0202-11, 60687-0202-21, 60687-0202-94, 60687-0213, 60687-0213-11, 60687-0213-21, 60687-0213-94 |
| Lot numbers | 174096 |
| Expiration dates | 2019-05-31 |
Product
Aripiprazole Tablets, USP, 10 mg, 100 Tablets (10 x 10) unit dose blisters [NDC60687-179-11; UPC (01) 003 60687 179 11 7] per carton (NDC 60687-179-01), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217.
Reason for recall
CGMP Deviations: lot made with active pharmaceutical ingredient that did not meet all its intended specifications.
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-0595-2018. 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.