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 ...

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 ...

Murraysville, Pa.-based Philips Respironics has issued a worldwide recall of its Trilogy Ventilators Models 100, 200 and 202 due to a potentially faulty component on the ventilators’ power boards. The ...

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 ...

Philips Respironics initiated a voluntary recall to address a potentially defective component on the Trilogy Ventilator power management board, which could affect the function of the device. If this ...

(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 ...

Respironics Inc, a division of Philips Healthcare, is recalling about 600 Philips Respironics Trilogy Ventilators worldwide because of a potentially defective component on the power board that could ...

FORT WORTH (CBSNewsTexas.com) — A massive recall of millions of sleep apnea machines that has dragged on for nearly two years has left many patients waiting with seemingly no good options. In June of ...

Philips Respironics recently announced a mandatory software correction and updates to its instructions for use (IFU) for the Trilogy Evo, EV300, Evo02, and Evo Universal ventilators to resolve several ...