BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 2132441 · Received June 14, 2011

    Report

    Report Number
    1824206-2011-03242
    Event Type
    Malfunction
    Date Received
    June 14, 2011
    Date of Event
    May 23, 2011
    Report Date
    May 23, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNTS MAINTENANCE STATED THE HEAD DOWN FUNCTION DID NOT WORK. HE USED A NEW PENDENT AT THE CONTROL BOX AND ALSO SWITCHED THE HEAD AND KNEE MOTOR CONNECTIONS AT THE CONTROL BOX TO ISOLATE THE ISSUE TO THE CONTROL BOX.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESIDENT BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1