Cordis DE Mexico
FDA adverse event reports naming Cordis DE Mexico as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CORDIS DE MEXICO.
- Total reports
- 15,476
- Deaths
- 1,121
- Injuries
- 8,887
- Malfunctions
- 5,430
Reports per year
1,68006
2,58707
2,75908
1,86109
1,02710
98711
76512
84113
61514
18616
35117
1818
1619
720
121
Source: FDA adverse event reports by year received, 2006–2021. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Coronary Drug-Eluting StentNIQ8,017
- Stent, CarotidNIM1,827
- Stents, Drains And Dilators For The Biliary DuctsFGE1,108
- Catheter, Intravascular, DiagnosticDQO642
- Catheter, Angioplasty, Peripheral, TransluminalLIT614
- Catheter, PercutaneousDQY562
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX535
- Stent, IliacNIO535
- Stent, CoronaryMAF471
- Filter, Intravascular, CardiovascularDTK295
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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