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
- 1,975
- Deaths
- 30
- Injuries
- 269
- Malfunctions
- 1,661
Reports per year
6409
12310
18311
38312
40613
52114
29515
Source: FDA adverse event reports by year received, 2009–2015. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA1,332
- Pump, InfusionFRN588
- Pump, Infusion, PcaMEA24
- Container, Specimen, SterileFMH12
- Filter, Infusion LineFPB7
- Ventilator, Continuous, Facility UseCBK6
- Syringe, PistonFMF3
- Tubing, Pressure And AccessoriesBYX1
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1
- Applicator, Absorbent Tipped, Non-SterileKXF1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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