Philips Respironics recalled 13,811 ventilators the company reworked or replaced after it pulled millions of them off the market in summer 2021. The devices — Trilogy 100, Trilogy 200, and Garbin Plus ...

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, ...

SANTA CLARA, Calif., Sept. 13, 2017 /PRNewswire/ -- Based on its recent analysis of the home ventilation market, Frost & Sullivan recognizes Philips with the 2017 North American Home Ventilation ...

More than a year into the repair-and-replace program for the 5.5 million CPAP and BiPAP machines and other ventilators recalled by Philips since June 2021, the Dutch devicemaker has identified a pair ...

(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 ...

The FDA cited Philips Healthcare ($PHG) subsidiary Philips Respironics with a Class 1 recall--the agency's most serious designation--for 600 of the company's Trilogy ...

Philips Respironics, a division of Philips Healthcare, has initiated a voluntary recall of its Trilogy Ventilator to address a potentially defective component on its power management board. Philips ...

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A Dutch manufacturer says it hopes to triple the production of hospital ventilators being assembled in Murrysville and Carlsbad, Calif., between now and the end of September. “In March, our production ...

Philips' Trilogy offer multiple ventilation modes, real time data sharing capabilities and a long battery life that allows patients to have a near normal quality of life. SANTA CLARA, California, Sept ...

Five years ago, the U.S. Department of Health and Human Services tried to plug a crucial hole in its preparations for a global pandemic, signing a $13.8 million contract with a Pennsylvania ...