WDTN

Millions of BiPAP, CPAP machine masks recalled; pose risk of death

(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 ...
Philadelphia Tribune

Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall

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 ...
FierceBiotech

Philips recalls 17M CPAP and BiPAP machine masks due to potential magnet interference

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 ...
WSOC-TV

FDA: Recalled Philips BiPAP, CPAP machines tied to more than 560 deaths

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 ...
FierceBiotech

Philips' CPAP and BiPAP mask recall stretches to 22M devices, lands Class I FDA label

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 ...
Business Wire

FDA EUA Makes First N99 Filter Patch Available for Use With CPAP and BIPAP

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 ...