BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3 MOTOR ADVANCE BED

    MDR report key: 1191314 · Received September 26, 2008

    Report

    Report Number
    1824206-2008-03472
    Event Type
    Malfunction
    Date Received
    September 26, 2008
    Date of Event
    August 29, 2008
    Report Date
    August 29, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HOSPITAL BIOMED REPORTED THAT THE CPR FEATURE DOES NOT FUNCTION ON THIS BED. AFTER TROUBLESHOOTING WITH A HILL-ROM SERVICE TECHNICIAN, IT WAS DETERMINED THAT THE CPR RELEASE CABLE WAS OUT OF ADJUSTMENT. HE ADJUSTED THE CPR RELEASE CABLE TO RESOLVE THE ISSUE. THERE WERE NO REPORTED ADVERSE EVENTS ASSOCIATED WITH THIS PRODUCT PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 3 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1130 NA

    Patients

    Seq Age Sex Outcome Treatment
    1