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Recall Observatory FDA recall evidence

Derived label

Device software or design

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
Software errors results in no low battery alarm/infusion stopping 4)Medium priority KVO/End of Infusion alarms may result in
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
CareFusion 303, Inc.

Field note

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