Just a few weeks after racking up its fifth Class I recall from the FDA this year, Philips has hit the half-dozen mark. Its sixth of the classifications—which denote the agency’s most serious rating ...

The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...

Philips CPAP and BiPap machines that were recalled in 2021 have since been linked to deaths and thousands of malfunctions, the FDA says Roberto Machado Noa/LightRocket via Getty The Food and Drug ...

As Philips still scrambles to wrap up its 2021 recall of more than 5.5 million ventilators and CPAP and BiPAP machines, a new issue has cropped up among another swath of its CPAP machines. The FDA ...

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

Three years after one of the largest medical device recalls in history, the fallout – health-wise and financial – continues to impact many patients with sleep apnea. Now a critical deadline is ...

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 ...