BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTA BED

    MDR report key: 2892531 · Received November 26, 2012

    Report

    Report Number
    1824206-2012-07701
    Event Type
    Malfunction
    Date Received
    November 26, 2012
    Date of Event
    November 2, 2012
    Report Date
    November 2, 2012
    Manufacturer
    HILL-ROM INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT WHEN THEY PRESS THE KNEE DOWN SWITCH THE KNEE WILL NOT RUN ALL THE WAY DOWN AND WHEN THE LET OFF THE KNEE DOWN SWITCH THE KNEE WILL RUN BACK UP A FEW INCHES. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTA BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 1600

    Patients

    Seq Age Sex Outcome Treatment
    1