Covidien, Formerly Nellcor
FDA adverse event reports naming Covidien, Formerly Nellcor as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN, FORMERLY NELLCOR.
- Total reports
- 2,580
- Deaths
- 7
- Injuries
- 441
- Malfunctions
- 2,126
Reports per year
21511
78112
1,15513
42914
Source: FDA adverse event reports by year received, 2011–2014. 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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