BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VASOVIEW HEMOPRO 2

    MDR report key: 3876140 · Received May 20, 2014

    Report

    Report Number
    2242352-2014-00572
    Event Type
    Malfunction
    Date Received
    May 20, 2014
    Date of Event
    April 21, 2014
    Report Date
    April 22, 2014
    Manufacturer
    MAQUET CARDIOVASCULAR, LLC
    Product Code
    GEI
    PMA / PMN Number
    K101274
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS RETURNED TO THE FACTORY FOR EVALUATION. IT SHOWED SIGNS OF CLINICAL USAGE AND EVIDENCE OF BLOOD. A VISUAL INSPECTION DETERMINED THAT THE HEATER WIRE WAS DETACHED FROM THE TIP OF THE HOT JAW. THE HEATER WIRE APPEARED PHYSICALLY DAMAGED AND WAS BENT AND TWISTED AWAY FROM THE HOT JAW. THIS PROBLEM IS CONSISTENT WITH AN IMPROPER INSERTION OF THE TOOL INTO THE CANNULA. BASED UPON THE RECEIVED CONDITION OF THE DEVICE, THE REPORTED COMPLAINT WAS CONFIRMED. A LOT HISTORY RECORD REVIEW COULD NOT BE PERFORMED AS THE PRODUCT LOT NUMBER IS UNKNOWN. INTERNAL CORRECTIVE ACTION (WY-2013-47) ISSUED FOR THIS FAILURE MODE. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING AN ENDOSCOPIC VEIN HARVESTING PROCEDURE, THE JAW ON THE VASOVIEW HEMOPRO 2 WAS BENT AND WAS UNABLE TO SEAL THE BRANCHES. A REPLACEMENT DEVICE WAS USED TO COMPLETE THE PROCEDURE. THE HOSPITAL DID NOT REPORT ANY PATIENT EFFECTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    298950 VASOVIEW HEMOPRO 2 ENDOSCOPIC VESSEL HARVESTING GEI MAQUET CARDIOVASCULAR, LLC VH-4000

    Patients

    Seq Age Sex Outcome Treatment
    1