Covidien, Formerly Nellcor Puritan
FDA adverse event reports naming Covidien, Formerly Nellcor Puritan as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN, FORMERLY NELLCOR PURITAN.
- Total reports
- 1,711
- Deaths
- 6
- Injuries
- 327
- Malfunctions
- 1,376
Reports per year
5511
36912
90913
37814
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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