BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 2024085 · Received March 11, 2011

    Report

    Report Number
    1824206-2011-01486
    Event Type
    Malfunction
    Date Received
    March 11, 2011
    Date of Event
    April 3, 2008
    Report Date
    April 3, 2008
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE HI VOLTAGE POWER CONTROL BOARD, THE HEAD SWITCH HOUSING ASSEMBLY, THE LOGIC BOARD AND THE TEST PORT CABLE ASSEMBLY TO RESOLVE THE ISSUE. THIS MDR IS A RESULT OF CAPA ACTIVITY FOR THE RETROSPECTIVE REVIEW OF COMPLAINTS.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE HI/LOW IS RUNNING DOWN ON ITS OWN. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1060

    Patients

    Seq Age Sex Outcome Treatment
    1