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Philips Disputes Additional Deaths Linked To May Recall Of Breathing Machines

 
• By Brian Bossetta

The US FDA is reporting dozens more additional deaths associated with a May recall of Philips ventilators than initially reported. The company says it stands by its original number of seven and has reached out to the FDA.

FDA HQ
• Source: Shutterstock: JHVEPhoto

In March, Philips initiated a recall of 100,000 BiPAP A30, BiPAP A40, BiPAP V30, and OmniLab Advanced Plus ventilators because problems with the alarms could cause the machines to shut down.

At the time, Medtech Insight reported 10 serious injuries and seven deaths linked to BiPAP A30 and A40, though no adverse events were linked to the V30 or OmniLab Advanced Plus machines

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