BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZX

    MDR report key: 1193110 · Received October 6, 2008

    Report

    Report Number
    9680128-2008-00159
    Event Type
    Malfunction
    Date Received
    October 6, 2008
    Date of Event
    September 12, 2008
    Report Date
    September 12, 2008
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Removal / Correction Number
    9680128-2008-001C
    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 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