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 ...
(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 ...
On Tuesday, Koninklijke Philips N.V. (NYSE:PHG) issued a correction related to the Software Version used in Trilogy Evo, Trilogy EV300, Trilogy Evo O2, and Trilogy Evo Universal ventilators to resolve ...
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 ...
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, ...