BEUDAMED
    FDA Adverse Event Death Summary report: N

    4 MOTOR ADVANCE BED P1155

    MDR report key: 1616604 · Received February 18, 2010

    Report

    Report Number
    1824206-2010-02629
    Event Type
    Death
    Date Received
    February 18, 2010
    Date of Event
    August 24, 2006
    Report Date
    August 24, 2006
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN CONDUCTED AN INVESTIGATION AND WAS UNABLE TO DUPLICATE THE ISSUE. THE DEVICE FUNCTIONED PROPERLY.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGES THAT THE BED EXIT DID NOT SEND A NURSE CALL SIGNAL TO THE NURSES STATION WHEN A PATIENT EXITED THE BED AND FELL. THE ACCOUNT STATED THAT THE PATIENT DIED. THE CORONER'S REPORT STATED THAT THE PATIENT'S DEATH WAS NOT A RESULT OF THE FALL, BUT A RESULT OF THE PATIENT'S CURRENT MEDICAL CONDITION. THE ACCOUNT WOULD NOT RELEASE ANY INFORMATION REGARDING THE PATIENT, NOR WOULD THE ACCOUNT RELEASE A COPY OF THE CORONER'S REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4 MOTOR ADVANCE BED P1155 A/C POWERED HOSPITAL BED FNL HILL-ROM RITTER P1155F55

    Patients

    Seq Age Sex Outcome Treatment
    1 Death