StarClose SE Vascular Closure System — Class II medical device recall Z-1202-2017
Terminated recall by Abbott Vascular, reported 2017-02-22, distributed in PR. Abbott Vascular is recalling the StarClose SE Vascular Closure System because it may exhibit difficulty or fai
| Recall number | Z-1202-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abbott Vascular, Temecula, CA, United States |
| Recall initiated | 2017-02-10 |
| Classified | 2017-02-15 |
| Reported by FDA | 2017-02-22 |
| Terminated | 2017-12-06 |
| Distributed | PR |
| Countries outside the US | CH, DE, ES, IT, SE |
| UPC / GTIN / UDI-DI | 08717648079467 |
| Model numbers | 14679-01, 14679-02, 50831K1, 50903K1, 50908K1, 50911K1, 50916K1, 50921K1, 50924K1, 50929K1, 51002K1, 51008K1, 5101241, 51013K1, 5101441, 51016K1, 5101941, 5102141, 51021K1, 51026K1, 5102741, 51029K1, 5103141, 51103K1, 5110541 and 43 more |
Product
StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.
Reason for recall
Abbott Vascular is recalling the StarClose SE Vascular Closure System because it may exhibit difficulty or failure to deploy the StarClose SE Clip.
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-1202-2017. 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.