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 US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...

MEMPHIS, Tenn.--(BUSINESS WIRE)--Azimuth Sleep Solutions has received FDA Emergency Use Authorization(EUA) for their patent-pending PortPatch™ product, in order to expand air filtration capabilities ...

As hospitals in New York City and beyond are facing a shortage of mechanical ventilators for COVID-19 patients in critical care, many are turning to readily available CPAP and BiPAP machines as a ...

Magnets in the recalled masks, used in breathing machines for sleep apnea, can interfere with pacemakers and other lifesaving medical devices. Philips Respironics has voluntarily recalled more than 17 ...

(RTTNews) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently conducted an ...

PHILADELPHIA, June 30, 2021 /PRNewswire/ — The national plaintiffs’ law firm Berger Montague has filed a class action lawsuit against Dutch medical equipment company Philips to protect consumers ...