BEUDAMED
    FDA Adverse Event Death Summary report: N

    WATCHCHILD OBSTETRICAL PATIENT DATA MONITORING SYS

    MDR report key: 283820 · Received June 23, 2000

    Report

    Report Number
    1045510-2000-00007
    Event Type
    Death
    Date Received
    June 23, 2000
    Date of Event
    August 20, 1999
    Report Date
    June 23, 2000
    Manufacturer
    HILL-ROM, INC.
    Product Code
    HGM
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PT'S UTERUS RUPTURED AND PT DIED. WATCHCHILD IN USE AT TIME OF DEATH. INCIDENT WAS NOT DUE TO FAILURE OF WATCHCHILD, IT WAS BEING USED TO MONITOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WATCHCHILD OBSTETRICAL PATIENT DATA MONITORING SYS PATIENT MONITORING SYSTEM HGM HILL-ROM, INC. 2519 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death