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 ...

Philips issued a voluntary recall of software for its series of Trilogy Evo ventilators as well as a warning for patients not to use non-pneumatic nebulizers with the devices because they may not ...

Philips’ Respironics division previously notified U.S. customers of the correction in mid-July, urging them to download and install version 1.05.10.00 for its Trilogy Evo, Trilogy EV300, Trilogy Evo ...

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 ...

Philips woes continue as they face yet another Class I voluntary recall for its Trilogy Evo ventilator in recent months. The device maker is instructing users to change filters more frequently to ...

(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 ...

In March, Philips recalled more than 73,000 ventilators that absorbed dust and dirt into breathing tubes. This week, the Food and Drug Administration reported that the issue has been associated with ...

Royal Philips NV has warned that some of its ventilators can malfunction with a sudden loss of power, the latest in a series of product safety issues plaguing the company. The medical equipment ...