BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLORENCE BED

    MDR report key: 1875053 · Received October 13, 2010

    Report

    Report Number
    9680128-2010-00148
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 15, 2010
    Report Date
    September 15, 2010
    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 BOARD DOES NOT FUNCTION AND THE CPR CYLINDER LEAKS. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLORENCE BED HOSPITAL BED, AC POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL23SE NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK