Carefusion Corp.
FDA adverse event reports naming Carefusion Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CAREFUSION CORP..
- Total reports
- 1,139
- Deaths
- 17
- Injuries
- 168
- Malfunctions
- 941
Reports per year
3309
8910
32511
20412
24213
19114
5415
117
Source: FDA adverse event reports by year received, 2009–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA734
- Pump, InfusionFRN364
- Pump, Infusion, PcaMEA20
- Ventilator, Continuous, Facility UseCBK6
- Filter, Infusion LineFPB5
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK2
- Container, Specimen, SterileFMH2
- Set, Blood TransfusionBRZ1
- Calculator, Predicted Values, Pulmonary FunctionBTY1
- Ventilator, Non-Continuous (Respirator)BZD1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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