BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTA BED

    MDR report key: 3073032 · Received April 6, 2013

    Report

    Report Number
    1824206-2013-01958
    Event Type
    Malfunction
    Date Received
    April 6, 2013
    Date of Event
    March 8, 2013
    Report Date
    March 8, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE LEFT LOWER PIVOT AT THE FOOT END OF THE SIDERAIL WAS BROKEN. THE CUSTOMER ORDERED A COMPLETE LEFT FOOT WELDMENT IN ORDER TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATED THE LEFT FOOT SIDERAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    142618 ADVANTA BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1600

    Patients

    Seq Age Sex Outcome Treatment
    1