BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 4230305 · Received November 6, 2014

    Report

    Report Number
    3008262382-2014-01879
    Event Type
    Malfunction
    Date Received
    November 6, 2014
    Report Date
    October 17, 2014
    Manufacturer
    INVACARE REHABILITATION EQUIP
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    ENDUSER IS REPORTING THAT THE LIFT IS LOSING PRESSURE, STATES THEY HAVE TO MOVE VERY QUICKLY AND HAVE RECENTLY QUIT USING DUE TO POTENTIAL FOR INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    713702 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE REHABILITATION EQUIP 9805P

    Patients

    Seq Age Sex Outcome Treatment
    1 Other