BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RAULAND-BORG

    MDR report key: 2830257 · Received November 6, 2012

    Report

    Report Number
    MW5027558
    Event Type
    Malfunction
    Date Received
    November 6, 2012
    Date of Event
    October 1, 2012
    Report Date
    November 6, 2012
    Manufacturer
    RAULAND-BORG
    Product Code
    ILQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    OUR NEWLY INSTALLED NURSE CALL SYSEM (RESPONDER 5) HAS BEEN CAUSING INTERFERENCE WITH OUR INFANT SECURITY SYSTEM (SAFE PLACE INFANT SECURITY SYSTEM) CAUSING MULTIPLE FALSE ALARMS. THE NURSE CALL SYSTEM IS EMITTING NOISE INTERFERENCE IN THE 260-370 MGH LEVEL. THE INFANT SECURITY SYSTEM WAS INSTALLED MANY YRS AGO AND HAS BEEN RELIABLE, HOWEVER WHEN THE NEW NURSE CALL SYSTEM WAS POWERED-UP, ALARMS BEGAN IMMEDIATELY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RAULAND-BORG NURSE CALL SYSTEM ILQ RAULAND-BORG

    Patients

    Seq Age Sex Outcome Treatment
    1 SAFE PLACE INFANT SECURITY SYSTEM -RF TECHNOLOGIES