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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Company Transitions from Infrastructure Buildout to Active Market Execution as Expanded 510(k) Review Enters Final ...

Longtime LPGA star Jane Park announced on Instragram that her daughter is struggling with pneumonia following a few years of ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. (WKBN) – More than 17 million masks for ...