BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2000046 · Received February 3, 2011

    Report

    Report Number
    1824206-2011-00637
    Event Type
    Malfunction
    Date Received
    February 3, 2011
    Date of Event
    January 11, 2011
    Report Date
    January 11, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND SERVICE CODE 30-49 AND LEFT INTERMEDIATE CABLE WITH INTERMITTENT CONNECTION. WAS NOT WORKING CORRECTLY DUE TO OLD FLUID RESIDUE IN UCM BOARD. REPLACED INTERMEDIATE CABLE AND UCM BOARD TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT RECEIVED THAT THE "SERVICE REQUIRED LIGHT" WAS FLASHING. NO ALLEGED INJURIES BY ACCOUNT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900AF1619

    Patients

    Seq Age Sex Outcome Treatment
    1