BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2222873 · Received July 15, 2011

    Report

    Report Number
    1824206-2011-03755
    Event Type
    Malfunction
    Date Received
    July 15, 2011
    Date of Event
    June 25, 2011
    Report Date
    June 25, 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

    TECH FOUND THE TRENDELENBURG VALVE WAS MISSING THE RUBBER END. THE TECH REMOVED THE RUBBER FROM INSIDE THE MANIFOLD BLOCK AND REPLACED THE TRENDELENBURG VALVE TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    TECH ALLEGED THAT THE BED WOULD NOT GO INTO TRENDELENBURG. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1