Cordis Angiographic Catheter Extensions — Class II medical device recall Z-0720-2023
Ongoing recall by Cordis US Corp, reported 2022-12-21, distributed nationwide. There is a potential for separation at the male connector.
| Recall number | Z-0720-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis US Corp, Miami Lakes, FL, United States |
| Recall initiated | 2022-11-07 |
| Classified | 2022-12-15 |
| Reported by FDA | 2022-12-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, BE, CZ, DE, ES, FR, GB, IE, IL, IS, JP, KR, NL, PT, RU |
| Lot numbers | 18062882, 18064731, 18064732, 18066535, 18069744, 18070824, 18072508, 18074058, 18076420, 18078225, 18079156, 18081307, 18083133, 18084892, 18086388, 18088193, 18097369, 18099118, 18101041, 18102623, 18104313, 18106093, 18108019, 18109512, 502-100D, 502-101D, 502-102D |
| Model numbers | 18062882, 18064731, 18064732, 18066535, 18069744, 18070824, 18072508, 18074058, 18076420, 18078225, 18079156, 18081307, 18083133, 18084892, 18086388, 18088193, 18097369, 18099118, 18101041, 18102623, 18104313, 18106093, 18108019, 18109512, 502-100D and 2 more |
Product
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
Reason for recall
There is a potential for separation at the male connector.
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-0720-2023. 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.