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 ...
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 ...
The federal judge in charge of the multidistrict litigation by users of Philips' recalled CPAP, Bi-Level PAP and mechanical ventilators has appointed, opens new tab two men and two women to serve as ...
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