BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    THERMOGRAPHY

    MDR report key: 12835705 · Received November 17, 2021

    Report

    Report Number
    MW5105450
    Event Type
    Malfunction
    Date Received
    November 17, 2021
    Date of Event
    November 15, 2021
    Report Date
    November 15, 2021
    Manufacturer
    UNK
    Product Code
    LHQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    (B)(6) DR (B)(6) CONTINUES TO USE THERMOGRAPHY TO "SCREEN" FOR CANCER ON MY MOTHER. (B)(6). (B)(6) IS A QUACK. SHUT HER DOWN. WHICH (B)(6) MISSED. AND LIKELY CONTRIBUTED TO HER HAVING CANCER DUE TO THE STEM CELL TREATMENTS SHE HAS GIVEN HER. FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1723888 THERMOGRAPHY SYSTEM, TELETHERMOGRAPHIC (ADJUNCTIVE USE) LHQ UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Female