Medical device maker Phillips formally entered into a consent decree that stops the company from selling sleep apnea machines in the United States over health concerns that include cancer. The decree ...

WASHINGTON — A device made by Philips Respironics for treating sleep apnea should be monitored closely when in use because it can overheat, according to federal regulators. The Food and Drug ...

The company behind a global recall of sleep apnea machines said Monday it will stop selling the devices in the U.S., under a tentative agreement with regulators that could cost the manufacturer nearly ...

Three years after one of the largest medical device recalls in history, the fallout – health-wise and financial – continues to impact many patients with sleep apnea. Now a critical deadline is ...

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 ...

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 ...

The FDA has received more than 500 reports of death tied to Philips’ recalled sleep apnea devices since 2021, according to a Jan. 31 agency update. The devicemaker recalled millions of ventilators and ...

Dutch medical device maker Philips said Monday it had reached a $1.1 billion deal to settle U.S. lawsuits over faulty sleep machines that have dogged the company. The company's shares initially soared ...