BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SUTURE TRIMMER

    MDR report key: 1914426 · Received December 3, 2010

    Report

    Report Number
    2953144-2010-03099
    Event Type
    Injury
    Date Received
    December 3, 2010
    Date of Event
    November 10, 2010
    Report Date
    November 10, 2010
    Manufacturer
    AV-REDWOOD CITY
    Product Code
    MGB
    PMA / PMN Number
    P960043
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Additional Manufacturer Narrative · 1

    (B)(4). THE CUSTOMER REPORTED THE DEVICE WAS DISCARDED. THE LOT NUMBER WAS NOT INDENTIFIED; THEREFORE, A DEVICE HISTORY RECORD REVIEW COULD NOT BE PERFORMED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE SYSTEM INTERMITTENTLY DISPLAYS THE DOSE VALUE AS EITHER 0 (ZERO) OR A DOSE VALUE THAT IS HIGHER THAN THE AVERAGE VALUE DISPLAYED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A RADIOLOGY TECHNICIAN TRAINED IN THE USE OF THE PROGLIDE DEVICE, ATTEMPTED ARTERIOTOMY CLOSURE OF THE COMMON FEMORAL ARTERY AFTER AN INTERVENTIONAL PROCEDURE. REPORTEDLY, THE TECHNICIAN WAS UNABLE TO ADVANCE THE KNOT FORWARD TO THE ARTERIOTOMY USING THE SUTURE TRIMMER. THE SUTURES WERE REMOVED AND HEMOSTASIS WAS ACHIEVED APPLYING MANUAL COMPRESSION FOR APPROXIMATELY 20 MINUTES. THERE WAS NO ADVERSE PATIENT EFFECT. THOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUTURE TRIMMER SUTURE MEDIATED CLOSURE MGB AV-REDWOOD CITY

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention