Magnets in the recalled masks, used in breathing machines for sleep apnea, can interfere with pacemakers and other lifesaving medical devices. Philips Respironics has voluntarily recalled more than 17 ...

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 ...

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 ...

Nearly five years after the Philips Respironics recall reshaped the CPAP market, respondents to a recent HME Newspoll say ...

BOSTON – Philips Respironics is recalling more than 17 million CPAP masks used by patients with sleep apnea. Magnets connect and hold the pieces of the mask in place, but the FDA said those magnets ...

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 ...