BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH

    MDR report key: 1120949 · Received August 13, 2008

    Report

    Report Number
    9680128-2008-00074
    Event Type
    Malfunction
    Date Received
    August 13, 2008
    Date of Event
    July 14, 2008
    Report Date
    July 14, 2008
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BED ALLEGEDLY DISPLAYED A "FOOT OVER RANGE" ERROR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP 2130000000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK