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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:120170

Artis zee systems x-ray, angiographic system

Official recall number

Z-0172-2014

Evidence summary

Product code
IZI
Recall status
Terminated
Event initiated
January 21, 2013
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0172-2014

Field note

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