BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MAQUET VASOVIEW HEMOPRO 2

    MDR report key: 10173783 · Received June 18, 2020

    Report

    Report Number
    MW5095076
    Event Type
    Malfunction
    Date Received
    June 18, 2020
    Date of Event
    June 16, 2020
    Report Date
    June 17, 2020
    Manufacturer
    MAQUET CARDIOVASCULAR LLC
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    MAQUET EVH VASOVIEW HEMOPRO 2 DEFECTIVE, END OF CLEAR LINE CAP MISSING ON SCOPE CARRIER. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    636152 MAQUET VASOVIEW HEMOPRO 2 ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI MAQUET CARDIOVASCULAR LLC 25150499

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR