The FDA is getting the word out on a mandatory software update from Philips for its Trilogy line of portable life support ventilators, used in both hospitals and the home. Philips’ Respironics ...

Respiratory medical device firm Philips has been hit with yet another Class I recall by the US Food and Drug Administration (FDA) after it was found that the software in some of its ventilators ...

AUBURN, Ala. (WRBL) – An Auburn University mechanical engineering group’s test to turn a CPAP machine into an emergency ventilator has passed a major test for use on a live animal. The … ...