The FDA announced that recalled CPAP and BiPAP machines have been tied to hundreds of deaths. The CPAP and BiPAP machines were initially recalled in June 2021. CPAP and BiPAP machines are both worn at ...

The company behind a global recall of sleep apnea machines said Monday it will stop selling the devices in the U.S., under a tentative agreement with regulators that could cost the manufacturer nearly ...

Philips Respironics is recalling some of its BiPAP machines, including the OmniLab Advanced +, due to a plastic that can contaminate the machine, according to the U.S. Food and Drug Administration ...

Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...

Philips Respironics is recalling some of its BiPAP machines due to a plastic that can contaminate the machine and cause it to fail, according to the U.S. Food and Drug Administration (FDA). The ...

In 2021, polyester-based polyurethane (PE-PUR) foam used in Philips Respironics ventilators, CPAP and BiPAP machines was found to degrade and cause serious health issues or death, leading to a mass ...