BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON-AC-POWERED PATIENT LIFT

    MDR report key: 4953840 · Received February 6, 2014

    Report

    Report Number
    3004859134-2014-00001
    Event Type
    Malfunction
    Date Received
    February 6, 2014
    Report Date
    February 6, 2014
    Manufacturer
    H FINE AND SON LTD
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PER IMPORTER'S MDR: 21-DEC-2012-RBS- THE DEALER REPORTED THAT THE FULL BODY LIFT PREMIER SLING STRAP WAS FRAYING. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    78524 NON-AC-POWERED PATIENT LIFT NON-AC-POWERED PATIENT LIFT FSA H FINE AND SON LTD

    Patients

    Seq Age Sex Outcome Treatment
    1 Other