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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:138818

RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray. Intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts.

Official recall number

Z-2390-2015

Evidence summary

Product code
IZL
Recall status
Terminated
Event initiated
July 13, 2015
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2390-2015

Field note

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