Philips Respironics Recalls Trilogy Ventilators Worldwide

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 defective piece may cause the ventilator to stop delivering mechanical breaths, potentially leading to patient death. So far, there have been no reports of deaths or serious injury related to this product recall.

The recall applies to Triology Ventilators shipped between Dec. 31, 2013 and Jan. 30, 2014.

More Articles on Recalls:

Medisca Recalls L-Citrulline Products, Cites Lack of L-Citrulline
Ben Venue Laboratories Recalls 10% Acetylcysteine Solution
FDA Recalls Covidien's Puritan Bennett 840 Ventilator

Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Whitepapers

Featured Webinars

>