The Food and Drug Administration (FDA) has issued a safety communication regarding the recall of certain Philips Respironics masks used with bilevel positive airway pressure (also known as Bi-Level ...

Millions of masks used with sleep apnea machines have been recalled for safety concerns. Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure or ...

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 ...

There is major medical recall involving machines many people use to sleep every night.The U.S. Food and Drug Administration announced Tuesday night they are recalling Phillips BiPAP and CPAP masks ...

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 ...

Talk to your physician or medical device provider first before stopping or changing how you use your product, as the benefits of using these devices may outweigh the risks for many users. Register ...