The U.S. Food and Drug Administration (FDA) has ordered a software recall for a type of ventilator, for fear of "serious injuries or death." The ventilators—the Philips Respironics, Inc. Trilogy EVO, ...

FDA today identified Philips Respironics Trilogy Evo continuous ventilator recall as Class I, over a month after the company initiated the voluntary correction in March. The ventilators affected by ...

Being on a ventilator can be a frightening experience for many patients, and switching between different ventilators for transport, or when going home, can be emotionally challenging as well. To make ...

BUT AS ACTION NEWS INVESTIGATOR PAUL VAN OSDOL TELLS US, THEY HAVEN’T MADE ANY VENTILATORS. PAUL? PAUL: 10,000 LOW COST VENTILATORS WERE SUPPOSED TO BE MADE AT THE PHILIPS RESPIRONICS PLANT HERE IN ...