Carefusion SD
FDA adverse event reports naming Carefusion SD as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CAREFUSION SD.
- Total reports
- 1,374,294
- Deaths
- 187
- Injuries
- 1,150
- Malfunctions
- 1,372,957
Reports per year
314
2115
2716
2217
7818
5219
78,46420
188,23921
871,32522
154,73423
37,08824
33,15725
11,08426
Source: FDA adverse event reports by year received, 2014–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN1,346,702
- Pump, Infusion, PcaMEA16,677
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK10,481
- OximeterDQA267
- Set, Administration, IntravascularFPA135
- Infusion Safety Management SoftwarePHC19
- Enteroscope And AccessoriesFDA9
- Cabinet, Table And Tray, AnesthesiaBRY1
- Syringe, PistonFMF1
- Accessories, Pump, InfusionMRZ1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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