Skip to content
Recall Observatory FDA recall evidence

Derived label

Device software or design

McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
Software Error
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Mckesson Information Solutions LLC

Field note

Send feedback

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