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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:198921

2D Perfusion, release R1.0.x, R1.1.x, R1.2, and R1.2.1

Official recall number

Z-1417-2023

Evidence summary

Product code
OWB
Recall status
Open, Classified
Event initiated
February 20, 2023
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1417-2023