Skip to content
Recall Observatory FDA recall evidence

Derived label

Device software or design

Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
software issue related to the date/time format. This connection issue
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Field note

Send feedback

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