The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics ... to the user that the DreamStation is not working the ...

The U.S. Food and Drug Administration on Friday announced the recall of certain Philips Respironics devices ... or indication to the user that the DreamStation is not working the way the doctor ...

Philips subsidiary Philips Respironics and an external medical panel. In June 2021, millions of sleep apnea masks were recalled because of a foam breakdown. “The new results indicate that ...

A device made by Philips Respironics for treating sleep apnea ... The Food and Drug Administration warned Tuesday that Philips' DreamStation 2 can start to smoke or even begin burning while ...

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 ...

The Food and Drug Administration issued a new warning for users of certain CPAP machines – the latest in a series of troubles for Philips Respironics ... of the Philips DreamStation 2, citing ...

More than 17 million masks containing magnetic clips have been distributed by unit Philips Respironics, the company said. The unit has received 14 reports of injuries following use of the masks as ...

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 ...

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG; AEX: PHIA) today provides an update on the comprehensive test and research program of its subsidiary Philips Respironics, following the ...

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 ...