BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTA

    MDR report key: 1964119 · Received December 21, 2010

    Report

    Report Number
    1824206-2010-11824
    Event Type
    Malfunction
    Date Received
    December 21, 2010
    Date of Event
    December 2, 2010
    Report Date
    December 2, 2010
    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

    TECHNICIAN ADVISED THE ACCOUNT TO CHECK CONNECTIONS AT THE TRANSFORMER UNDER THE ELECTRONICS PAN. THE BED WAS IN THE BED SHOP AT THE TIME THE ALLEGED FLASH WAS SEEN. NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THIS BED AT THIS TIME.

    Description of Event or Problem · 1

    ACCOUNT STATED THE BED IS SHOWING AN ERROR CODE. THE ACCOUNT REPLACED THE FUSE ON THE AIR BOARD. AFTER REPLACING THE AIR BOARD, THE ACCOUNT SAW A FLASH FROM UNDER THE BED AND ERROR CODE IS AGAIN ACTIVE. ACCOUNT STATED THE SAME FUSE IS AGAIN COMPROMISED. NO INJURIES REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1