BEUDAMED
    FDA Adverse Event Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3022079 · Received March 26, 2013

    Report

    Report Number
    1531186-2013-01292
    Date Received
    March 26, 2013
    Report Date
    February 26, 2013
    Manufacturer
    NEW PROKIN
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    USER ALLEGED THAT THE SLING IS RIPPING AWAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    124516 NON AC-POWERED PATIENT LIFT 880.5510 FSA NEW PROKIN R100

    Patients

    Seq Age Sex Outcome Treatment
    1 Other