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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:212211

muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate

Official recall number

Z-1069-2025

Evidence summary

Product code
DRT
Recall status
Open, Classified
Event initiated
April 22, 2024
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1069-2025

Field note

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