Skip to content
Recall Observatory FDA recall evidence

Derived label

Device software or design

GE Healthcare, CARESCAPE Monitor B850, B650 or B450. Patient Monitor.

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
software version 2 the PDM may not start communicating to the monitor and loss of the PDM parameters could
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
GE Healthcare, LLC

Field note

Send feedback

We'll only use this to respond to your feedback.