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 ...

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 ...

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 ...

PHILLIPS HAS NOW RECALLED ALMOST 20 DIFFERENT MODELS OF CPAP AND BIPAP MACHISNE BECSEAU OF HEALTH CONCERNS. THE COMPANY SAYS THAT THE PHONE THAT IS INSIDE OFHE T MACHINES TO DAMPEN THE SOUND CAN BREAK ...

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 ...

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 ...

A North Texan, navigating the recall of some CPAP and BiPAP machines made by Philips Respironics, learned the company says it’s too old to repair. Read on for how she found a resolution. For years, ...

BATON ROUGE, La. (WAFB) - The U.S. Food and Drug Administration is alerting patients, caregivers and healthcare providers Philips Respironics (Philips) recalled certain masks due to a safety concern.

The gold standard for moderate to severe obstructive sleep apnea (OSA) is continuous positive airway pressure (CPAP) therapy. For a CPAP machine alone, it can cost anywhere from $500 to $1000 or more.

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 ...