BEUDAMED
    FDA Adverse Event Other Summary report: N

    THE FLORENCE BED

    MDR report key: 1770349 · Received July 20, 2010

    Report

    Report Number
    9680128-2010-00088
    Event Type
    Other
    Date Received
    July 20, 2010
    Date of Event
    June 22, 2010
    Report Date
    June 23, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    AFTER INVESTIGATION, NO INJURY HAPPENED - NO FINGERS WERE BROKEN.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE HEAD LEFT SIDE RAIL WAS BENT. IT WAS REPORTED THAT THE SPACE BETWEEN THE RAILS WAS LIMITED. IT WAS REPORTED THAT THE PT BROKE THEIR FINGER WHILE ATTEMPTING TO EXIT THE BED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK