BEUDAMED
    FDA Adverse Event Summary report: N

    POWERED PATIENT ROTATION BED

    MDR report key: 3830754 · Received May 23, 2014

    Report

    Report Number
    1531186-2014-01958
    Date Received
    May 23, 2014
    Date of Event
    April 14, 2014
    Report Date
    April 14, 2014
    Manufacturer
    LAND AMERICA HEALTH & FITNESS
    Product Code
    IKZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PROVIDER ALLEGES THE RAIL FOR THE BED IS BENT CAUSING IT NOT TO SLIDE UP AND DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    308902 POWERED PATIENT ROTATION BED 890.5225 IKZ LAND AMERICA HEALTH & FITNESS 5310IVC

    Patients

    Seq Age Sex Outcome Treatment
    1 Other