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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:203364

F2-01 Frame, physiological patient monitor (with arrhythmia detection or alarms)

Official recall number

Z-2656-2023

Evidence summary

Product code
MHX
Recall status
Open, Classified
Event initiated
September 08, 2023
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2656-2023

Field note

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