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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:181040

Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.

Official recall number

Z-1933-2020

Evidence summary

Product code
OWB
Recall status
Terminated
Event initiated
April 10, 2020
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1933-2020

Field note

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