Cordis Cashel
FDA adverse event reports naming Cordis Cashel as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CORDIS CASHEL.
- Total reports
- 4,718
- Deaths
- 87
- Injuries
- 3,496
- Malfunctions
- 1,135
Reports per year
1916
1,01417
1,62418
1,67819
31220
521
1622
2523
2224
225
126
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Filter, Intravascular, CardiovascularDTK2,759
- Catheter, Angioplasty, Peripheral, TransluminalLIT987
- Catheter, Intravascular, DiagnosticDQO681
- Stents, Drains And Dilators For The Biliary DuctsFGE138
- Dilator, EsophagealKNQ41
- System, Endovascular Graft, Aortic Aneurysm TreatmentMIH39
- Coronary Drug-Eluting StentNIQ32
- Catheter, PercutaneousDQY10
- Wire, Guide, CatheterDQX7
- Stent, IliacNIO7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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