BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MERIT CUSTOM KIT

    MDR report key: 2192935 · Received July 21, 2011

    Report

    Report Number
    1721504-2011-00231
    Event Type
    Malfunction
    Date Received
    July 21, 2011
    Date of Event
    June 17, 2011
    Report Date
    June 28, 2011
    Manufacturer
    MERIT MEDICAL SYSTEMS, INC.
    Product Code
    DTL
    PMA / PMN Number
    K934123
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE EVAL: THE SUSPECT DEVICE HAS NOT BEEN RETURNED FOR EVAL. THE CUSTOMER DID NOT SPECIFY IF THIS WAS THE INITIAL USE OF THE DEVICE. EVALUATION CONCLUSIONS: A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE EVAL HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT DURING AN ANGIOGRAPHIC PROCEDURE, THE ROTATOR ON THE STOPCOCK BROKE. THE CUSTOMER STATED THAT THE ROTATOR WAS STIFF WHILE CONNECTING IT TO A CATHETER. NO HARM OR INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MERIT CUSTOM KIT CATHETER, INTRAVASCULAR, DIAGNOSTIC DTL MERIT MEDICAL SYSTEMS, INC. F751156

    Patients

    Seq Age Sex Outcome Treatment
    1 CATHETER