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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:138999

Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.

Official recall number

Z-0766-2016

Evidence summary

Product code
KPR
Recall status
Terminated
Event initiated
July 22, 2015
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0766-2016

Field note

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