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 ...

The U.S. Food and Drug Administration is alerting patients, caregivers and health care providers that Philips Respironics has recalled certain BiPAP and CPAP masks due to a serious safety concern. The ...

(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 ...

Vitacore has received a Medical Device License (MDL) from Health Canada for FormFit, a fully custom-fit medical-grade silicone CPAP mask, the first of its kind, the company says.

Philips has recalled more than 17 million CPAP and BiPAP masks because the product’s magnets can interfere with implanted metal medical devices, such as pacemakers. As of Sept. 6, there have been 14 ...

Vitacore, a deep technology company, today announced that it has received a Medical Device Licence (MDL) from Health Canada for FormFit™, the world’s first fully custom-fit medical-grade silicone CPAP ...

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 ...

As competitor Philips continues to grapple with the effects of its long-standing recall of continuous positive airway pressure (CPAP) machines and other respiratory devices, ResMed is now issuing a ...

Dr. Chelsea Kadish and Kyle Goodknight explain why EMS providers who consider prehospital pediatric CPAP too aggressive should embrace the modality as safe and effective for even the youngest patients ...

It’s notoriously difficult for some sleep apnea patients to adapt to using a CPAP machine – but most will and should be given ...