Cordis S — Class II medical device recall Z-1826-2017
Terminated recall by Cordis Corporation, reported 2017-04-26. Deployment Difficulty.
| Recall number | Z-1826-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis Corporation, Miami Lakes, FL, United States |
| Recall initiated | 2017-02-16 |
| Classified | 2017-04-15 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2019-08-06 |
| Countries outside the US | AR, AT, AU, BE, BG, BR, CH, CL, CN, CO, CR, CZ, DE, ES, FI, FR, GB, IL, IR, IT, JO, KR, KW, NL, NZ, PL, PT, RS, SA, SE, SG, SI, TH, TR, TW, ZA |
| Quantity | 2,700 |
| UPC / GTIN / UDI-DI | 20705032066409, 20705032066829, 20705032066836, 20705032067024 |
| Lot numbers | 34469, 34470, 34551, 34552, 34585, 34586, 34587, 34588, 34589, 34823, 3487534993, 35006, 35009, 35068, 35069, 35077, 35165, 35199, 35228, 35229, 35287, 35352, 35361, 35469, 35470, 35500, 35568, 35597, 35706, 35707, 35715, 35716, 35741, 35742, 35755, 35756, 35823, 35824, 35859, 35860 and 106 more |
| Model numbers | SF05200MV, SF05200SV, SF06200MV, SF06200SV |
Product
Cordis S.M.A.R.T. Flex Vascular Stent System
Reason for recall
Deployment Difficulty.
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-1826-2017. 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.