Carefusion, Inc
FDA adverse event reports naming Carefusion, Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CAREFUSION, INC.
- Total reports
- 6,826
- Deaths
- 110
- Injuries
- 1,929
- Malfunctions
- 4,785
Reports per year
2715
3,18216
1,63817
15418
21219
28720
31721
17422
28423
15824
28525
10826
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Ventilator, Continuous, Facility UseCBK4,114
- Apparatus, Suction, Patient CareDWM539
- Lavage, JetFQH260
- Ventilator, High FrequencyLSZ218
- Applicator, Absorbent Tipped, SterileKXG172
- Anesthesia Conduction KitCAZ144
- Thoracentesis TrayPXI130
- Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term IndwellingPNG119
- Applicator, Absorbent Tipped, Non-SterileKXF108
- Laparoscope, General & Plastic SurgeryGCJ106
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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