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Pair Of Deaths Linked To Recalled Vyaire Medical Respiratory Devices

 
• By Brian Bossetta

The US FDA has labelled a recall of more than 6 million Airlife respiratory support devices class I. The recall covers devices manufactured in 2017 or earlier that can fail to provide adequate ventilation.

RECALL
• Source: Shutterstock

Vyaire Medical initiated a recall in December of various models of its Airlife Manual Resuscitator, a single patient use device designed to provide respiratory support. 

In total, the company recalled 6,633,173 resuscitators made in 2017 or earlier as well as some

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