ZEE Aspirin 325mg — Class II drug recall D-0041-2015
Terminated recall by Zee Medical Products Inc, reported 2014-10-29, distributed nationwide. Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive
| Recall number | D-0041-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zee Medical Products Inc, Irvine, CA, United States |
| Recall initiated | 2014-10-07 |
| Classified | 2014-10-22 |
| Reported by FDA | 2014-10-29 |
| Terminated | 2015-04-24 |
| Distributed | Nationwide (US) |
| Quantity | 43,752 boxes |
| Reason classes | undeclared allergen, labeling |
| Lot numbers | AK5172, AK5425, AK5548, AK5865, AK5963, AK6047, AK6114, AK6175, AK6346, AK6438, AK7062 |
Product
ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528
Reason for recall
Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.
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-0041-2015. 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.