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