BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 2914706 · Received January 14, 2013

    Report

    Report Number
    3004493922-2013-00117
    Event Type
    Malfunction
    Date Received
    January 14, 2013
    Report Date
    January 14, 2013
    Manufacturer
    INVACARE SUZHOU
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    THE END USERS DAUGHTER HAS REPORTED THAT THE LIFT LOWERS ON IT'S OWN WHEN THE END USER IS NOT IN IT. NO INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    20106 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

    Patients

    Seq Age Sex Outcome Treatment
    1 Other