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 ...

Despite recent test results showing that the disintegrating polyester-based polyurethane (PE-PUR) foam at the heart of Philips ongoing respiratory device recall “is unlikely to result in an ...

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 ...

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 ...

In partnership with Pittsburgh Post-Gazette. The massive recall of DreamStation machines and other breathing devices disrupted medical care for millions in the United States and around the world.