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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:163420

AirLife Resuscitation, Replacement kit for outer shell, Broselow Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.

Official recall number

Z-1579-2018

Evidence summary

Product code
OEV
Recall status
Terminated
Event initiated
April 27, 2017
Root cause
Component design/selection
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-1579-2018

Field note

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