BEUDAMED
    FDA Adverse Event Summary report: N

    AC-POWERED PATIENT LIFT

    MDR report key: 2955925 · Received February 11, 2013

    Report

    Report Number
    1531186-2013-00537
    Date Received
    February 11, 2013
    Report Date
    February 11, 2013
    Manufacturer
    NEW PROKIN
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4). THE DEALER REPORTED THAT THE 9042 STANDARD SLING STITCHING WAS COMING APART. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    59473 AC-POWERED PATIENT LIFT 880.5500 FNG NEW PROKIN 9042

    Patients

    Seq Age Sex Outcome Treatment
    1 Other