Some 70 incident reports potentially related to the affected machines were received by the Health Products Regulatory ...

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 ...

A doctor in Washington was sentenced to a year in jail for a scheme involving recalled Philips CPAP machines. Sleep ...

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 ...

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 ...

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 ...

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 ...

JACKSONVILLE, Fla — Troy Bouk is seeing firsthand what he believes are health impacts of recalled CPAP devices. “We are seeing tumors on the tongue and back of the throat,” Bouk said. “A lot of ...

Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...

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, ...

Sleep medicine specialist was sentenced to a year in prison and will pay $350K in restitut ...