BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLORENCE BED

    MDR report key: 1052200 · Received May 21, 2008

    Report

    Report Number
    9680128-2008-00012
    Event Type
    Malfunction
    Date Received
    May 21, 2008
    Date of Event
    April 22, 2008
    Report Date
    April 22, 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 HEAD ACTUATOR TUBE INTERFERES WITH THE BRAKE LEVER CAUSING THE BRAKES TO DISENGAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLORENCE BED HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL23E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA