BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VASOVIEW 7 XB

    MDR report key: 3851024 · Received February 12, 2014

    Report

    Report Number
    2242352-2014-00107
    Event Type
    Malfunction
    Date Received
    February 12, 2014
    Date of Event
    January 20, 2014
    Report Date
    January 21, 2014
    Manufacturer
    MAQUET CARDIOVASCULAR, LLC
    Product Code
    GEI
    PMA / PMN Number
    K041981
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT YET BEEN RETURNED TO MAQUET CARDIAC SURGERY FOR EVAL. WE ARE FOLLOWING UP WITH THE CUSTOMER FOR THE RETURN OF THE DEVICE. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED. A LOT HISTORY RECORD REVIEW WAS COMPLETED FOR THE REPORTED PRODUCT LOT NUMBER. THERE WAS NO NON-CONFORMANCE RECORDS IN THE LOT HISTORY. (B)(4).

    Description of Event or Problem · 1

    THE HOSP REPORTED THAT DURING THE BEGINNING OF AN ENDOSCOPIC VENIN HARVESTING PROCEDURE, AFTER CONNECTING THE INSUFFLATION TUBING TO THE BTT SHORT PORT/TROCAR ON THE VASOVIEW 7 XB, THE HARVESTER COULD NOT GET THE CO2 TO FLOW THROUGH BTT PORT/TROCAR. A REPLACEMENT DEVICE WAS USED TO COMPLETE THE PROCEDURE. THE HOSP DID NOT REPORT ANY PT EFFECTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    93131 VASOVIEW 7 XB GEI MAQUET CARDIOVASCULAR, LLC C-VH-3200 25089255

    Patients

    Seq Age Sex Outcome Treatment
    1 NI