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 ...

Philips has issued a voluntary recall of software for its Trilogy Evo ventilator ser | Philips issued a voluntary recall of ...

Last month, Philips issued a huge recall of ventilators and continuous positive airway pressure machines, leaving millions of people with sleep apnea unsure of how they’ll get a good night’s sleep.

FILE - Jeffrey Reed, who experienced persistent sinus infections and two bouts of pneumonia while using a Philips CPAP machine, poses with the device at his home, Oct. 20, 2022, in Marysville, Ohio.

NEW YORK — The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders. The FDA said ...

The company responsible for a global recall of sleep apnea machines will be barred from resuming production at U.S. facilities until it meets a number of safety requirements, under a long-awaited ...