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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:124803

Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The intended use of the oxygen sensor is to provide the oxygen concentration of the delivered gas at the patient wye (inspiratory-expiratory interface). The oxygen sensor does not control the oxygen level or the flow of gases. The intended use of the devices is as critical care ventilators that provide continuous mechanical ventilation for patients.

Official recall number

Z-0821-2014

Evidence summary

Product code
CBK
Recall status
Terminated
Event initiated
January 25, 2013
Root cause
Labeling Change Control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0821-2014

Field note

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