BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CERASORB

    MDR report key: 6208603 · Received December 23, 2016

    Report

    Report Number
    MW5066910
    Event Type
    Injury
    Date Received
    December 23, 2016
    Date of Event
    September 9, 2010
    Report Date
    December 23, 2016
    Manufacturer
    ABBOTT/ SPINAL CONCEPTS
    Product Code
    LYC
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HAD AN MRI WITH MAGNEVIST APPROVED BY MOLINA CAUSED CERASORB DENTAL IMPLANT CEMENT IN MY LUMBAR SPINE FUSION SURGERY TO SPREAD THROUGHOUT MY BODY AND DAMAGED MY NERVES SEVERELY ON TOP OF BEING A VICTIM OF (B)(6)HOSPITAL OF (B)(6) WITH NEVER FDA APPROVED PEEK ORGANIC PLASTIC L4-L5 S1 - THROUGH MY BACK MUSCLES PLUS OTHER DEVICES AND MATERIALS IN MY SPINE, BACK AND NECK, I'VE HAD YEARS OF DOCTORS LYING TO ME AND (B)(6) CONFLICT OF INTEREST FRAUDULENT PHONY SCANDALOUS AKA DOCTOR GOT WORKER COMPENSATION ON MY AUTOMOBILE ACCIDENT. I STILL HAVE HIS EVALUATION FROM THE AUTOMOBILE ACCIDENT REPORT HE WROTE...(B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    852657 CERASORB CERASORB LYC ABBOTT/ SPINAL CONCEPTS

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR Other| S