Cordis MAXI LD PTA Dilatation Catheter — Class II medical device recall Z-0250-2020
Terminated recall by Cordis Corporation, reported 2019-11-06, distributed in AL, AZ, FL, MN, MO. Product was manufactured utilizing an expired inner body.
| Recall number | Z-0250-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis Corporation, Miami Lakes, FL, United States |
| Recall initiated | 2019-10-04 |
| Classified | 2019-10-30 |
| Reported by FDA | 2019-11-06 |
| Terminated | 2020-12-14 |
| Distributed | AL, AZ, FL, MN, MO |
| Quantity | 21 units |
| Lot numbers | 82169860 |
| Model numbers | 4171460S |
| Expiration dates | 2020-10-31 |
Product
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Reason for recall
Product was manufactured utilizing an expired inner body.
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/Z-0250-2020. 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.