Just a few months after kicking off a June 2021 recall that would ultimately grow to encompass 5.5 million respiratory devices, Philips began a repair-and-replace program to fix the affected CPAP and ...

A U.S. federal court has officially ordered Philips to restrict the production and sale of its CPAP and BiPAP ventilators for sleep apnea. The move is the culmination of a years-long international ...

More than 15 million devices worldwide were voluntarily recalled by Philips after it was revealed a noise-canceling foam inside could break down and be inhaled by the user while they sleep. Stream NBC ...

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 ...

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 ...

AMSTERDAM, Oct 6 (Reuters) - The U.S. Food and Drug Administration (FDA) said it is still not satisfied with how Dutch healthcare technology company Philips (PHG.AS), opens new tab has handled a major ...

WASHINGTON — 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 ...

The move comes as Philips has agreed to a consent decree with the Food and Drug Administration and the Department of Justice that could cost the company nearly $400 million. In June 2021, Philips ...