Sleep apnea is a medical condition that affects an estimated 22 million Americans. Typical symptoms of sleep apnea include heavy snoring, excessive daytime sleepiness or fatigue, and difficulty with ...

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 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 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 ...

Electronics manufacturing giant Philips is recalling millions of CPAP and BiPAP devices due to an issue that could potentially pose a health risk to users of the machines. In the wake of the recall, ...

WASHINGTON — Medical equipment company Philips Respironics has recalled at least 17 million masks used with breathing devices designed to treat patients with sleep apnea and other respiratory ...

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 ...