BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZX

    MDR report key: 1121228 · Received August 16, 2008

    Report

    Report Number
    9680128-2008-00083
    Event Type
    Malfunction
    Date Received
    August 16, 2008
    Date of Event
    July 18, 2008
    Report Date
    July 18, 2008
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

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

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZX HOSPITAL BED, A-C-POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP 2140000000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK