BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HENRY SCHEIN

    MDR report key: 14349579 · Received May 10, 2022

    Report

    Report Number
    2411236-2022-00002
    Event Type
    Injury
    Date Received
    May 10, 2022
    Date of Event
    February 21, 2022
    Report Date
    April 26, 2022
    Manufacturer
    PRIMA DENTAL GROUP
    Product Code
    EJL
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    FL, US
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    THE DENTIST WAS PERFORMING A PROCEDURE ON A 64 YEAR OLD MALE PATIENT WHEN THE BUR CAME OUT OF A HANDPIECE AND WAS SWALLOWED BY THE PATIENT. ABDOMINAL RADIOGRAPHS WERE DONE INITIALLY AND CT SCAN AT A LATER DATE TO MAKE SURE THE BUR PASSED THE STOOL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    870789 HENRY SCHEIN CARBIDE SURGICAL BUR FG 557 EJL PRIMA DENTAL GROUP

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Male Other