(RTTNews) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently conducted an ...

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 ...

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.

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 ...

HERE’S INVESTIGATIVE REPORTER PAUL VAN OSDOL. THE RECALL AFFECTED MILLIONS OF BREATHING MACHINES MADE BY PHILIPS, WHICH HAS OFFICES HERE IN BAKERY SQUARE AND IN MORRISVILLE. ON SATURDAY, DON SCHREIBER ...

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 ...

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