(RTTNews) - Philips Respironics, affiliated to Dutch consumer electronics giant, announced additional usage instructions for Trilogy Evo Ventilators related to use of in-line nebulizers. The company ...

90,905 ventilators recalled globally due to software errors causing potential safety risks. Nine injuries and one death reported; Philips requires urgent software updates. Memorial Day Special: Access ...

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, ...

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 ...

Philips Respironics Inc., of Murrayville, Pa., was compelled to engage in multiple recalls over the use of a supplier’s polyester-based polyurethane (PE-PUR) sound abatement foam, and the latest ...

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 ...

Philips has received 542 reports about this issue, according to the FDA. PHG shares were up 0.48% at $21.13 during the premarket session on the last check Tuesday. 3 Summer "Power Patterns" Are About ...