(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 ...
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 ...
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, ...
Koninklijke Philips PHG notified its customers about a possible power malfunction in itsTrilogy Evo continuous ventilators and initiated a software update to resolve the same in March. The FDA ...
This story was originally published on MedTech Dive. To receive daily news and insights, subscribe to our free daily MedTech Dive newsletter. Philips recalled several models of its Trilogy ventilators ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback