BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN TOUCH ZX

    MDR report key: 2123209 · Received June 13, 2008

    Report

    Report Number
    9680128-2008-00015
    Event Type
    Malfunction
    Date Received
    June 13, 2008
    Date of Event
    May 13, 2008
    Report Date
    May 13, 2008
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BED READ "TILT ERROR CODE" AND COULD NOT BE LOWERED, ONLY BE RAISED.

    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