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 ...

Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

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 ...

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 ...

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Medical device maker Philips is recalling sleep apnea machines and ventilators containing foam that could put users at risk of cancer or other health issues. The Dutch company announced a U.S. recall ...

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 ...