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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:121286

Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures

Official recall number

Z-2160-2013

Evidence summary

Product code
KXJ
Recall status
Terminated
Event initiated
August 02, 2013
Root cause
Radiation Control for Health and Safety Act
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2160-2013

Field note

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