Ferrous Sulfate 325 MG tablet — Class III drug recall D-0810-2018
Terminated recall by Aidarex Pharmaceuticals LLC, reported 2018-05-23, distributed in FL. Presence of Foreign Tablets/Capsules
| Recall number | D-0810-2018 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aidarex Pharmaceuticals LLC, Corona, CA, United States |
| Recall initiated | 2018-04-10 |
| Classified | 2018-05-15 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2019-12-04 |
| Distributed | FL |
| Quantity | 450 bottles |
| NDC | 33261-0715-00 |
| Lot numbers | 57909-1, 57909-2 |
| Expiration dates | 2019-04-30, 2019-06-30 |
Product
Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00
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-0810-2018. 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.