BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PERCLOSE PROGLIDE

    MDR report key: 17855380 · Received September 29, 2023

    Report

    Report Number
    MW5146344
    Event Type
    Injury
    Date Received
    September 29, 2023
    Date of Event
    June 30, 2020
    Report Date
    September 26, 2023
    Manufacturer
    ABBOTT VASCULAR
    Product Code
    MGB
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    I HAD A SURGERY AT (B)(6) MEDICAL CENTER IN (B)(6). I REALIZED IN THE MIDDLE OF MY SURGERY THAT I GOT SCAMMED BY THE DOCTORS. NOT ONLY DID I GET SCAMMED, BUT THE PRODUCT FAILED. I HAD TO LISTEN TO THE DOCTOR SAVE MY LIFE. AFTER MY SURGERY THEY DIDN'T TELL ME ABOUT THE PRODUCT FAILURE, OR ABOUT THE BLOOD LOSS. THEY SENT ME HOME AS IF NOTHING HAPPENED HOWEVER, I WAS AWAKE DURING THE FAILURE. I JUST COULDN'T GET MY EYES OPEN, I WOKE UP A FEW TIMES DURING MY SURGERY. THE PERCLOSE PROGLIDE MADE BY ABBOTT VASCULAR INC IS A DANGEROUS PRODUCT THAT GETS STUCK AND ALLOWS PEOPLE TO HEMORRHAGE FOR A LONG PERIOD OF TIME. I NEED THE FDA TO SEE THE PHOTOS OF MY BODY SO YOU CAN UNDERSTAND. I BLED AND BLED WHILE LISTENING TO THE DOCTOR SCREAMING ABOUT HOW THE BLEEDING WOULDN'T STOP. MY SURGERY REPORT IS A LIE. I WAS ON THE TABLE FOR 5.5 HOURS FOR SOMETHING THAT SHOULD HAVE ONLY TAKEN 90 MINUTES. I NEED THE FDA TO STEP IN AND DO SOMETHING ABOUT THE DOCTORS AND THE PRODUCT BECAUSE PEOPLE ARE GOING TO DIE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1568550 PERCLOSE PROGLIDE DEVICE, HEMOSTASIS, VASCULAR MGB ABBOTT VASCULAR

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Female Other