BEUDAMED
    FDA Adverse Event Summary report: N

    POWERED PATIENT ROTATION BED

    MDR report key: 3081569 · Received April 29, 2013

    Report

    Report Number
    1531186-2013-01799
    Date Received
    April 29, 2013
    Report Date
    April 3, 2013
    Manufacturer
    LAND AMERICA HEALTH & FITNESS
    Product Code
    IKZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    (B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. THE FACILITY REP ALLEGED THAT THERE IS A SHORT IN THE WIRE BECAUSE IF YOU MOVE THE WIRE, IT WILL WORK AND NOW IT WON'T WORK AT ALL. THE BED WILL NOT GO UP OR DOWN. MDR FILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    185954 POWERED PATIENT ROTATION BED 890.5225 IKZ LAND AMERICA HEALTH & FITNESS 5310IVC

    Patients

    Seq Age Sex Outcome Treatment
    1 Other