Cordis Europa, N.V.
FDA adverse event reports naming Cordis Europa, N.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CORDIS EUROPA, N.V..
- Total reports
- 3,717
- Deaths
- 296
- Injuries
- 1,636
- Malfunctions
- 1,757
Reports per year
597
2098
2899
1400
1701
902
52203
1,06704
60605
8806
43307
28208
28209
26710
7711
Source: FDA adverse event reports by year received, 1997–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Angioplasty, Peripheral, TransluminalLIT1,334
- Coronary Drug-Eluting StentNIQ1,162
- Stents, Drains And Dilators For The Biliary DuctsFGE471
- Filter, Intravascular, CardiovascularDTK302
- Stent, CoronaryMAF182
- Catheter, Intravascular, DiagnosticDQO83
- Catheter, PercutaneousDQY42
- Stent, IliacNIO29
- Stent, RenalNIN25
- Dilator, EsophagealKNQ24
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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