BEUDAMED
    FDA Adverse Event Other Summary report: N

    KIN-COM II

    MDR report key: 189232 · Received September 25, 1998

    Report

    Report Number
    1022819-1998-00001
    Event Type
    Other
    Date Received
    September 25, 1998
    Date of Event
    January 23, 1998
    Report Date
    September 24, 1998
    Manufacturer
    CHATTANOOGA GROUP, INC.
    Product Code
    IKK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    PHYSICAL THERAPIST

    Narratives

    Description of Event or Problem · 1

    EMPLOYEE AT PHYSICAL THERAPY CLINIC WANTED TO EXPERIENCE AN ECCENTRIC CONTRACTION ON KIN-COM DYNAMOMETER. DURING EXERCISE, HER PATELLA DISLOCATED. PATELLA WAS RESET IMMEDIATELY. DEVICE WAS OPERATING WITHIN ITS NORMAL OPERATING PARAMETERS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KIN-COM II ISOKINETIC TESTING & EVALUATION SYSTEM IKK CHATTANOOGA GROUP, INC. 5030 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other