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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:111193

EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.

Official recall number

Z-2072-2012

Evidence summary

Product code
MQB
Recall status
Terminated
Event initiated
June 19, 2012
Root cause
Radiation Control for Health and Safety Act
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2072-2012