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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:199976

bellavista 1000e Ventilator, Catalogue Number 301.100.130; Continuous Use Ventilator

Official recall number

Z-1967-2023

Evidence summary

Product code
CBK
Recall status
Completed
Event initiated
May 05, 2023
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1967-2023

Field note

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