BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 2050826 · Received April 4, 2011

    Report

    Report Number
    1824206-2011-02004
    Event Type
    Malfunction
    Date Received
    April 4, 2011
    Date of Event
    March 10, 2011
    Report Date
    March 10, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN ASKED ACCOUNT TO ISOLATE THE PENDANT, THE AUTO CONTOUR, AND THE LOCKOUT BOX. THE ACCOUNT PLUGGED THE PENDANT INTO THE CONTROL BOX AND THE PROBLEM RETURNED. THE ACCOUNT REPLACED THE CONTROL BOX TO CORRECT THE ISSUE.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE HEAD SECTION WOULD NOT LOWER. NO REPORT OF INJURY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1