BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PERCLOSE PROGLIDE

    MDR report key: 1221943 · Received October 24, 2008

    Report

    Report Number
    1221943
    Event Type
    Malfunction
    Date Received
    October 24, 2008
    Date of Event
    October 6, 2008
    Report Date
    October 20, 2008
    Manufacturer
    ABBOTT VASCULAR DEVICES
    Product Code
    MGB
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DEVICE DID NOT CONTAIN SUTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PERCLOSE PROGLIDE VASCULAR CLOSURE DEVICE MGB ABBOTT VASCULAR DEVICES * 690436H

    Patients

    Seq Age Sex Outcome Treatment
    1 *