BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2132572-1999-00044

    MDR report key: 257546 · Received December 30, 1999

    Report

    Report Number
    2132572-1999-00044
    Event Type
    Malfunction
    Date Received
    December 30, 1999
    Date of Event
    November 24, 1999
    Report Date
    December 23, 1999
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    AT A RESCUE, THE AED DELIVERED ONE SHOCK THEN THE AED POSTED A "CALL FOR SERVICE".

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other