BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT VASCULAR PERCLOSE

    MDR report key: 1005329 · Received February 26, 2008

    Report

    Report Number
    MW5005742
    Event Type
    Malfunction
    Date Received
    February 26, 2008
    Date of Event
    February 25, 2008
    Report Date
    February 25, 2008
    Manufacturer
    ABBOTT VASCULAR
    Product Code
    MGB
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    A PLUNGER WOULD NOT ADVANCE MORE THAN 3/4 DOWN INTO TRACK. (PER MD).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT VASCULAR PERCLOSE 6F STAR CLOSE MGB ABBOTT VASCULAR 6F STAR CLOSE 59176-6H

    Patients

    Seq Age Sex Outcome Treatment
    1