Aspirin DR Enteric Coated Tablets — Class III drug recall D-1483-2014
Terminated recall by Mckesson Packaging Services, reported 2014-08-06, distributed nationwide. Failed Dissolution Specification; at the 12 month time interval.
| Recall number | D-1483-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Packaging Services, Concord, NC, United States |
| Recall initiated | 2014-06-19 |
| Classified | 2014-07-28 |
| Reported by FDA | 2014-08-06 |
| Terminated | 2017-04-27 |
| Distributed | Nationwide (US) |
| Quantity | 1,511,250 tablets |
| Reason classes | specification failure |
| Lot numbers | 0093943 |
Product
Aspirin DR Enteric Coated Tablets, USP 325 mg, UD 750 tablets (25x30), Dist. By: McKesson Packaging Services a business unit of McKesson Corporation, concord, NC
Reason for recall
Failed Dissolution Specification; at the 12 month time interval.
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-1483-2014. 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.