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 ...

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 ...

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 ...

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 ...

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 ...

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

In a Nov. 28 safety alert, the FDA warned patients and healthcare providers to carefully monitor Philips machines used for obstructive sleep apnea after receiving reports that the machines have shown ...

HERE’S INVESTIGATIVE REPORTER PAUL VAN OSDOL. THE RECALL AFFECTED MILLIONS OF BREATHING MACHINES MADE BY PHILIPS, WHICH HAS OFFICES HERE IN BAKERY SQUARE AND IN MORRISVILLE. ON SATURDAY, DON SCHREIBER ...