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Home » Philips BiPAP Sees Class I Recall Related to 952 Injuries, 65 Deaths
Philips BiPAP Sees Class I Recall Related to 952 Injuries, 65 Deaths
Several Philips BiPAP devices and certain Baxter Life2000 ventilator systems are under FDA Class I recalls, the most serious type of recall, as use of the devices can result in serious injury or death.