BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ON-Q

    MDR report key: 2493845 · Received March 4, 2012

    Report

    Report Number
    MW5024656
    Event Type
    Injury
    Date Received
    March 4, 2012
    Date of Event
    July 15, 2003
    Report Date
    March 4, 2012
    Manufacturer
    I-FLOW CORPORATION
    Product Code
    MEB
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    LA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    PT COMPLAINS HE HAS HAD MORE THAN 10 SURGERIES ON HIS RIGHT SHOULDER. THE FIRST AND SECOND SURGERIES HE USED ON-Q WHICH CAUSED HIS CHONDROLYSIS. THIS CAUSED HIM TO HAVE A RIGHT SHOULDER REPLACEMENT SURGERY. THIS HAS BROUGHT HIM SO MUCH PAIN, STRESS AND SUFFERING

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ON-Q ON-Q PAIN MANAGEMENT SYSTEM MEB I-FLOW CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR