BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FIRST SAVE

    MDR report key: 220950 · Received April 23, 1999

    Report

    Report Number
    2132572-1999-00009
    Event Type
    Malfunction
    Date Received
    April 23, 1999
    Date of Event
    April 1, 1999
    Report Date
    April 23, 1999
    Manufacturer
    SURVIVALINK CORP
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    A REPAIR OF AN AED REVEALED THE SONARALERT WAS NOT OPERATING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FIRST SAVE AUTOMATED EXTERNAL DEFIBRILLATOR (AED) LDD SURVIVALINK CORP 9100-001 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other