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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:187573

Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029, 722035, 722038, and 722058.

Official recall number

Z-1904-2021

Evidence summary

Product code
OWB
Recall status
Terminated
Event initiated
June 23, 2016
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1904-2021