BEUDAMED
    FDA Adverse Event Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3961022 · Received July 28, 2014

    Report

    Report Number
    1531186-2014-02798
    Date Received
    July 28, 2014
    Report Date
    May 26, 2014
    Manufacturer
    FINE GROUP
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PROVIDER ALLEGES THE SLING IS RIPPING IN THE BACK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    439398 NON AC-POWERED PATIENT LIFT 880.5510 FSA FINE GROUP 2478445

    Patients

    Seq Age Sex Outcome Treatment
    1 Other