BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTA BED

    MDR report key: 2112892 · Received May 25, 2011

    Report

    Report Number
    1824206-2011-02878
    Event Type
    Malfunction
    Date Received
    May 25, 2011
    Date of Event
    May 2, 2011
    Report Date
    May 3, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN INDICATED THAT WHEN THE PATIENT WAS BEING MOVED, IT MAY HAVE CAUSED THE SIDERAIL TO BEND OUTWARD WHICH DAMAGED THE SLIDE BRACKET BADLY. HE FOUND THAT THE SIDERAIL WAS LATCHED IN THE INTERMEDIATE POSITION. HE STATED THE SIDERAIL UNLATCHED AND DROPPED INTO THE INTERMEDIATE POSITION. THE TECHNICIAN REPLACED THE SLIDE BRACKET TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE RIGHT HEAD SIDERAIL FELL WHEN THE PATIENT WAS MOVED AND A NURSE STRAINED HER BACK WHILE HOLDING THE PATIENT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK