BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1162756 · Received September 8, 2008

    Report

    Report Number
    1824206-2008-03329
    Event Type
    Malfunction
    Date Received
    September 8, 2008
    Date of Event
    August 13, 2008
    Report Date
    September 5, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CSR FOUND THE RIGHT UCM HEAD UP WOULD NOT WORK, FOUND SIDERAIL HAD SIGNS OF PAST FLUID EGRESS (CONTAMINATION) THAT HAD DRIED ON THE RIGHT UCM BOARD, NO INJURY OR INCIDENT REPORTED. CSR REPLACED THE RIGHT UCM BOARD TO RESOLVE THIS ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1900 P1900AF1619

    Patients

    Seq Age Sex Outcome Treatment
    1