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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:192375

Revolution CT, Revolution CT ES

Official recall number

Z-0816-2022

Evidence summary

Product code
JAK
Recall status
Open, Classified
Event initiated
June 30, 2021
Root cause
Radiation Control for Health and Safety Act
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0816-2022