Skip to content
Recall Observatory FDA recall evidence

Derived label

Device software or design

Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
software anomalies
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Orthosoft, Inc. dba Zimmer CAS

Field note

Send feedback

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