The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...

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 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 ...

Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...

There is major medical recall involving machines many people use to sleep every night.The U.S. Food and Drug Administration announced Tuesday night they are recalling Phillips BiPAP and CPAP masks ...

In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

It’s been just over a year since Randy Boyd was diagnosed with cancer. In July 2020, he felt a bruise on the left side of his neck and went to the doctor. A biopsy revealed it was throat cancer. “I ...

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.

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 ...