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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:141343

GE Precision MPi is an all-digital multipurpose tilt-C x-ray system, intended for a multitude of diagnostic procedures, including radiology, fluoroscopy, interventional procedures, vascular and non-vascular procedures, and specialized applications including angiographic studies.

Official recall number

Z-0753-2016

Evidence summary

Product code
OWB
Recall status
Terminated
Event initiated
July 01, 2008
Root cause
Radiation Control for Health and Safety Act
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0753-2016

Field note

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