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 ...

In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

Orlando, Florida — Carrie Markham spent three years struggling to breathe, suffering from lung problems that began in March of 2020, puzzling her doctors. "They just kept saying, 'We just don't know,' ...

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 ...

Federal regulators are heightening their warning about devices made by Philips Respironics used to treat obstructive sleep apnea, saying the products "may cause serious injuries or death." Philips ...

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 ...

An online reviewer is warning about a CPAP machine recall. He claims The Philips Dreamstation CPAP device, recalled in 2023, is still being used and could pose a cancer risk to users. Featured Video ...

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...