BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LABORATORY BURET KIMAX KG33 KIMBLE

    MDR report key: 10188768 · Received June 23, 2020

    Report

    Report Number
    MW5095160
    Event Type
    Injury
    Date Received
    June 23, 2020
    Date of Event
    October 17, 2017
    Report Date
    June 19, 2020
    Manufacturer
    DWK LIFE SCIENCES LLC
    Product Code
    GIO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    RI, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    INFLAMMATION NEUROTOXIN; LABORATORY ACCIDENT INVOLVING BOROSILICATE GLASS TUBING PRODUCT ARTICLE MADE FROM KG 33 CATASTROPHIC FAILURE SEVERE DERMAL INJURY GLASS NEEDLE LIKE SLIVERS IN SPINE AREA AND SHOULDER SEVERE LUNG INJURY FROM RESPIRABLE BIOACTIVE SILICA METAL OXIDE NANOPARTICLES. I'M NOT SEEKING PAIN PILLS I'M SEEKING TREATMENT TO GET BETTER. RECENT DEVELOPMENT OF SYSTEMIC TOXICITY INCLUDING ENDOCRINE DISRUPTION NEUROLOGICAL DISRUPTION METABOLIC DISRUPTION COGNITIVE ISSUES AND SEVERE DEGRADATION OF VISION. I WAS EXTREMELY HEALTHY AND VERY PHYSICALLY FIT AND ACTIVE RAN 5 MILES A DAY CANNOT FUNCTION DUE TO INJURY FROM GLASS SLIVERS IN THE SPINE AREA AND BREATHING ISSUES FROM A LONG INJURY ACUTE SILICOSIS FROM MASSIVE RESPIRABLE EXPOSURE TO MAKE SILICA DUST INCLUDING MULTIWALL CARBON NANOTUBES AND METAL OXIDE PARTICLES, HAVING SEVERE SYSTEMIC TOXICITY ISSUES AND IN DESPERATE NEED OF MEDICAL TREATMENT. WILLING TO TRAVEL IF NECESSARY TO FIND AN APPROPRIATE MEDICAL DOCTOR OR CLINIC. FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    646716 LABORATORY BURET KIMAX KG33 KIMBLE TUBE, COLLECTION, CAPILLARY BLOOD GIO DWK LIFE SCIENCES LLC 17026F10

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Hospitalization| O| R| S