BEUDAMED
    FDA Adverse Event Death Summary report: N

    BURKE

    MDR report key: 311585 · Received January 10, 2001

    Report

    Report Number
    1919278-2001-00001
    Event Type
    Death
    Date Received
    January 10, 2001
    Date of Event
    December 29, 2000
    Manufacturer
    BURKE, INC.
    Product Code
    FNJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT IS ALLEGED THAT SIDE RAIL WAS LAYING ON FLOOR. PT FELL ON SIDE RAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1006 BURKE OBESE BED FNJ BURKE, INC. BURKE TRI-FLEX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death