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 ...

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, ...

As of last month, according to its second-quarter earnings report, Philips has produced around 99% of the repair kits and replacement devices needed to remediate its massive respiratory device recall, ...

In March, Philips recalled more than 73,000 ventilators that absorbed dust and dirt into breathing tubes. This week, the Food and Drug Administration reported that the issue has been associated with ...