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 ...

In the race to provide the ventilators needed to treat COVID-19, several companies have developed new devices. But there may be a simpler approach. Formlabs has received an emergency use authorization ...

NEW YORK--(BUSINESS WIRE)--Nanotronics today announced that it has developed and designed nHale™, a bi-level positive air pressure (BIPAP) device to support spontaneously breathing adults weighing ...

Northwell Health said it has started to convert bi-level positive airway pressure machines into ventilators for COVID-19 patients. BiPAP machines usually are used for patients who have chronic ...

(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 ...

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 ...

"This latest recall raises further safety concerns both for Philips devices already subject to a recall, as well as additional devices," said Jeff Shuren, M.D., J.D., director of the FDA's Center for ...