BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    MDR report key: 1251338 · Received December 3, 2008

    Report

    Report Number
    2953144-2008-01943
    Event Type
    Injury
    Date Received
    December 3, 2008
    Date of Event
    October 20, 2008
    Report Date
    November 12, 2008
    Manufacturer
    ABBOTT VASCULAR - REDWOOD CITY
    Product Code
    MGB
    PMA / PMN Number
    P960043
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE IS EXPECTED TO BE RETURNED FOR EVALUATION. THE LOT NUMBER WAS PROVIDED. REVIEW OF THE DEVICE HISTORY RECORD IS FORTHCOMING. A FOLLOW-UP WILL BE SUBMITTED WITH ANY RELEVANT INFO. DEVICE #1 PROGLIDE, PART# 12673-03, LOT# 69076-6H, IS BEING FILED UNDER MEDWATCH MANUFACTURER REPORT NUMBER: 2953144-2008-01942.

    Description of Event or Problem · 1

    DEVICE #2 MALFUNCTION: CUFF MISS. TIME OF DEVICE MALFUNCTION DURING VESSEL CLOSURE. SYMPTOMS/AE: FAILURE TO ACHIEVE HEMOSTASIS. IT WAS REPORTED THAT A PHYSICIAN TRAINED IN THE USE OF THE PERCLOSE PROGLIDE DEVICE ATTEMPTED ARTERIOTOMY CLOSURE OF THE COMMON FEMORAL ARTERY AFTER AN INTERVENTIONAL PROCEDURE. REPORTEDLY, WHEN THE NEEDLE PLUNGER WAS REMOVED A NEEDLE TIP DID NOT CAPTURE A CUFF. A SECOND PERCLOSE PROGLIDE DEVICE WAS ATTEMPTED BUT ANOTHER CUFF MISS OCCURRED. A THIRD PROGLIDE WAS USED TO SUCCESSFULLY ACHIEVE HEMOSTASIS. NO ADVERSE PATIENT EFFECTS WERE REPORTED. NO ADDITIONAL INFO WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM MGB ABBOTT VASCULAR - REDWOOD CITY NA 69076-6H

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention DEVICE #1 PROGLIDE