Cordis Santa Clara
FDA adverse event reports naming Cordis Santa Clara as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CORDIS SANTA CLARA.
- Total reports
- 2,809
- Deaths
- 13
- Injuries
- 390
- Malfunctions
- 2,406
Reports per year
27117
43118
67519
42720
41121
41022
12223
3024
3225
Source: FDA adverse event reports by year received, 2017–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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