Skip to content
Recall Observatory FDA recall evidence

Derived label

Device software or design

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
Software anomaly that causes a false display of error
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
IPG Medical Corporation

Field note

Send feedback

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