BEUDAMED
    FDA Adverse Event Injury Summary report: N

    4251676

    MDR report key: 4251676 · Received October 15, 2014

    Report

    Report Number
    4251676
    Event Type
    Injury
    Date Received
    October 15, 2014
    Date of Event
    October 13, 2014
    Report Date
    October 15, 2014
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AZ, US

    Narratives

    Description of Event or Problem · 1

    UNABLE TO READ THE SCREEN OF THE ZOLL DEFIBRILLATOR DURING AN ATTEMPT TO DEFIB A PATIENT. THIS IS THE SECOND TIME IT HAS MALFUNCTIONED. IT HAS BEEN PULLED OUT OF USE.

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention