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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:180937

Positron Emission Tomography and Computed Tomography System, Model: uMI 550, Material Number: 88000057 - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and disorders in, but not limit to, oncology, cardiology and neurology.

Official recall number

Z-2819-2020

Evidence summary

Product code
KPS
Recall status
Terminated
Event initiated
March 26, 2020
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2819-2020