BEUDAMED
    FDA Adverse Event Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3072008 · Received April 22, 2013

    Report

    Report Number
    1531186-2013-01714
    Date Received
    April 22, 2013
    Report Date
    March 27, 2013
    Manufacturer
    NEW PROKIN
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CONSUMER ALLEGES THE SLING IS SHREDDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    172432 NON AC-POWERED PATIENT LIFT 880.5510 FSA NEW PROKIN R117

    Patients

    Seq Age Sex Outcome Treatment
    1 Other