Get all the latest news on coronavirus and more delivered daily to your inbox. Sign up here. As doctors face a shortage of ventilators that are crucial for treating coronavirus patients with ...

The U.S. Food and Drug Administration is alerting patients, caregivers and health care providers that Philips Respironics has recalled certain BiPAP and CPAP masks due to a serious safety concern. The ...

(WKBN) – More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration. The FDA said that Philips Respironics (Philips) has recalled ...

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 ...

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 ...

WASHINGTON - Philips Respironics has recalled more than 17 million masks used for people with sleep apnea and other respiratory issues due to a safety issue with magnets that could affect certain ...

The trouble seemingly never ends for Philips’ beleaguered Respironics division. Since beginning a recall of around 5.5 million ventilators and other breathing support machines more than a year ago, in ...