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 ...

As Philips reaches a consent decree agreement with the FDA that will temporarily suspend its sales of sleep therapy devices in the U.S., competitor ResMed, meanwhile, is ramping up its product ...

Obstructive apneic events during sleep are rare in healthy children, with findings from studies showing very low rates of occurrence, often fewer than 1 event per hour, and duration of events ...

Managing obstructive sleep apnea (OSA) can lead to a significant improvement in quality of life, with continuous positive airway pressure (CPAP) therapy playing a pivotal role. Understanding the ...

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 ...

UPDATE (2024-07-05): Update on Philips Respironics recall of several models of CPAP and BiLevel PAP machines and mechanical ventilators Once consumers have completed the registration process, they ...