BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3960926 · Received July 28, 2014

    Report

    Report Number
    3008262382-2014-00382
    Event Type
    Malfunction
    Date Received
    July 28, 2014
    Date of Event
    June 20, 2014
    Report Date
    June 20, 2014
    Manufacturer
    INVACARE REHABILITATION EQUIP
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    PER END USER FRONT 3 INCH CASTER WILL NOT SWIVEL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    437890 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE REHABILITATION EQUIP GHS350

    Patients

    Seq Age Sex Outcome Treatment
    1 Other