Add Yahoo as a preferred source to see more of our stories on Google. (Reuters) - The U.S. Food and Drug Administration said on Tuesday that medical device maker Philips has recalled certain masks ...

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 ...

Philips Respironics issued a warning that some of its sleep therapy masks used with its respiratory machines could pose a "risk of serious injury" to patients. Certain CPAP or Bi-Level PAP therapy ...

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 ...

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 ...

Millions of masks used with sleep apnea machines have been recalled for safety concerns. Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure or ...

The U.S. Food and Drug Administration said on Tuesday that medical device maker Philips has recalled certain masks used with some of its respiratory machines due to potential risk of serious injury.