Friday, February 9, 2018

US FDA News: HeartStart MRx Defibrillator by Philips Electronics: Class I Recall - Defects in Gas Discharge Tubes May Cause Device Failure

Continued use of the device in AED mode after failure may lead to serious patient injury or death.
Read more: HeartStart MRx Defibrillator by Philips Electronics: Class I Recall - Defects in Gas Discharge Tubes May Cause Device Failure