FDA Says Philips Respironics Recalls Some Trilogy Ventilators(1)

(Updates to add link in 6th bullet to previous story on Philips.)

• The US Food and Drug Administration says Philips Respironics is recalling some of its Trilogy EVO continuous ventilators due to a software-related possible power malfunction.
• The product names are Trilogy EVO, Trilogy EV300, Trilogy Evo O2, and Trilogy Evo Universal
• The products were distributed from March 20, 2019 to February 16, 2024
• Devices recalled in the US total 90,905
• Philips Respironics is providing a software update for its Trilogy Evo continuous ventilators to rectify the problem
• NOTE: From April 2024, Philips Warns of Faulty Ventilators Amid Mounting Safety ...