Carefusion 203, Inc
FDA adverse event reports naming Carefusion 203, Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CAREFUSION 203, INC.
- Total reports
- 1,290
- Deaths
- 55
- Injuries
- 236
- Malfunctions
- 997
Reports per year
109
8210
9911
12812
22613
27414
40715
7316
Source: FDA adverse event reports by year received, 2009–2016. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
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Recent recalls
No recalls listed in the FDA device recall database for this entry.
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