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 ...

Sleep apnea is a medical condition that affects an estimated 22 million Americans. Typical symptoms of sleep apnea include heavy snoring, excessive daytime sleepiness or fatigue, and difficulty with ...

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 ...

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

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, ...

Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...

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 ...

If you use a Philips CPAP machine, you have another thing to keep you awake at night: The FDA issued a warning Tuesday to patients and health care providers saying the company’s DreamStation 2 ...