BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC MED/SURG BED

    MDR report key: 1132363 · Received August 22, 2008

    Report

    Report Number
    9680128-2008-00089
    Event Type
    Malfunction
    Date Received
    August 22, 2008
    Date of Event
    July 24, 2008
    Report Date
    July 24, 2008
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A PATIENT FELL DUE TO A BRAKE FAILURE ON THE BED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK