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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:131436

Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators are microprocessor-controlled, electrically powered mechanical ventilators. Intended for use by medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients.

Official recall number

Z-0485-2015

Evidence summary

Product code
CBK
Recall status
Terminated
Event initiated
October 29, 2014
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0485-2015

Field note

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