BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT VASCULAR PERCLOSE PROGLIDE

    MDR report key: 18266939 · Received December 4, 2023

    Report

    Report Number
    MW5148753
    Event Type
    Malfunction
    Date Received
    December 4, 2023
    Date of Event
    November 29, 2023
    Report Date
    November 30, 2023
    Manufacturer
    ABBOTT VASCULAR
    Product Code
    MGB
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PERCLOSE DEVICE FAILED IN RIGHT FEMORAL ARTERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2177797 ABBOTT VASCULAR PERCLOSE PROGLIDE DEVICE, HEMOSTASIS, VASCULAR MGB ABBOTT VASCULAR 3100441

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Male