Inspiration Ventilator Recall News
On December 7, 2015, the U.S. Food and Drug Administration (FDA) announced that eVent Medical had issued a recall of their LS, 5i, or 7i Inspiration ventilators due to a device flaw that may cause the machine to turn off without alarm. For a device that may provide breath for people who have lost ability to breathe on their own, a device failure such as this could have been especially hazardous; however, the company received only one report of this issue occurring, with no reported injuries or deaths.
The Inspiration ventilator recall was initiated due to a faulty switch on the ventilators’ power board, which caused the ventilator to shut down without sounding an alarm.
OBTAIN A FREE MEDICAL DEVICE LAWSUIT EVALUATION FROM THE WEINBERG LAW FIRM
If you are a loved one has been seriously injured by a medical device, and you have a question concerning your legal rights, please submit our easy-to-use “Legal Case Evaluation Form”, or contact us toll free at 1-877-934-6274 for a free legal case evaluation.
Inspiration Ventilator Recall Information
The Inspiration ventilator recall includes all models of eVent Medical LS, 5i and 7i Inspiration ventilators distributed between February 14, 2013 and December 31, 2014, as well as all models manufactured before to January 21, 2015.