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 ...

The Food and Drug Administration has announced the recall of 150 MRI machines made by Philips. The recall is a correction and not a removal. The Panorama 1.0T HFO machine helps doctors make diagnoses ...

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 ...

(Reuters) -The U.S. FDA said on Thursday it has classified a recall of Philips' medical imaging machines as most serious due to the risk of a detector in some devices unexpectedly falling on patients ...

Philips is recalling the Tack endovascular system because of what it says are user challenges that have led to additional interventions needed to retrieve or remove the implant. The US Food and Drug ...