The trouble seemingly never ends for Philips’ beleaguered Respironics division. Since beginning a recall of around 5.5 million ventilators and other breathing support machines more than a year ago, in ...

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 — Medical equipment company Philips Respironics has recalled at least 17 million masks used with breathing devices designed to treat patients with sleep apnea and other respiratory ...

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 ...

Pittsburgh, Pennsylvania – Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting users of certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps ...

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 Respironics has recalled some face masks used with CPAP and BiPap machines because they have magnetic headgear clips that can interfere with other medical devices. The recalled masks are the ...

BATON ROUGE, La. (WAFB) - The U.S. Food and Drug Administration is alerting patients, caregivers and healthcare providers Philips Respironics (Philips) recalled certain masks due to a safety concern.