BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GEN 4 CALL LIGHT

    MDR report key: 4253560 · Received November 7, 2014

    Report

    Report Number
    MW5039072
    Event Type
    Malfunction
    Date Received
    November 7, 2014
    Date of Event
    November 5, 2014
    Report Date
    November 7, 2014
    Manufacturer
    CURBELL MEDICAL
    Product Code
    ILQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    CALL LIGHT PENDANT FAILED -- SENT BACK TO MANUFACTURER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    718478 GEN 4 CALL LIGHT CALL LIGHT ILQ CURBELL MEDICAL NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR