BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZX

    MDR report key: 1082755 · Received July 22, 2008

    Report

    Report Number
    9680128-2008-00055
    Event Type
    Malfunction
    Date Received
    July 22, 2008
    Date of Event
    June 26, 2008
    Report Date
    June 26, 2008
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, 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