BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1945233 · Received December 10, 2010

    Report

    Report Number
    1824206-2010-11521
    Event Type
    Malfunction
    Date Received
    December 10, 2010
    Date of Event
    November 12, 2010
    Report Date
    November 12, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE CPR CABLE WAS ADJUSTED TOO TIGHT AND CAUSED A JERKY MOVEMENT OF THE HEAD SECTION AND A DRIFT. THE TECHNICIAN ADJUSTED THE CPR CABLE TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE HEAD SECTION WILL BARELY RAISE AND DRIFTS DOWN WHEN YOU LET GO OF THE BUTTON.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1