There is a risk of serious injury or death related to more than 20 million CPAP masks made by ResMed, the FDA said Jan. 11. The continuous positive airway pressure masks, branded as AirFit and ...

SleepRes announced today that it received FDA 510(k) clearance for its Kricket PAP device for treating obstructive sleep ...

While we all know that getting enough sleep is important, the quality is just as critical as the duration. And poor-quality sleep could be due to sleep apnea, which beyond causing daytime fatigue is ...

Please provide your email address to receive an email when new articles are posted on . The FDA has granted de novo clearance to SoClean 3+, an over-the-counter bacterial reduction device for certain ...

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 ...

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 ...

Obstructive sleep apnea can cause or contribute to high blood pressure, so a new study examined which sleep apnea treatments – a CPAP machine or a mouthguard that keeps the airways open – was more ...

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 ...

If you use a continuous positive airway pressure (CPAP) machine for obstructive sleep apnea (OSA), you may breathe better at night. But you may also have dry mouth in the morning. Dry mouth is a ...