BEUDAMED
    FDA Adverse Event Death Summary report: N

    X-RAY

    MDR report key: 22035095 · Received May 16, 2025

    Report

    Report Number
    MW5170457
    Event Type
    Death
    Date Received
    May 16, 2025
    Date of Event
    May 10, 2025
    Report Date
    May 12, 2025
    Manufacturer
    UNK
    Product Code
    KPR
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    003
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    (B)(6) ANIMAL SERVICES, IS SAID TO HAVE XRAY MACHINES, HOWEVER THEY HAVE STATED THAT THEIR MACHINE HAS BEEN UNFUNCTIONAL FOR WEEKS, DESPITE THAT, MDAS HAS MISDIAGNOSED SEVERAL DOGS LEADING TO DEATH. THEY DO NOT HAVE A FUNCTIONAL XRAY MACHINE BUT HAVE EUTHANIZED SEVERAL DOGS STATING THEY SAW RADIOGRAPHS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1683902 X-RAY SYSTEM, X-RAY, STATIONARY KPR UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Life Threatening| D