Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:190138

Artis Q.zen biplane with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number:10848355

Official recall number

Z-0305-2022

Evidence summary

Product code
OWB
Recall status
Terminated
Event initiated
October 20, 2021
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0305-2022

Field note

Send feedback

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