BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EMA

    MDR report key: 18079381 · Received November 6, 2023

    Report

    Report Number
    3003928050-2023-00003
    Event Type
    Injury
    Date Received
    November 6, 2023
    Report Date
    October 9, 2023
    Manufacturer
    THE MYERSON COMPANY LIMITED
    Product Code
    LRK
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    B2: THIS HARM WAS NOT CONSIDERED TO BE AN ADVERSE EVENT SINCE THE INCIDENT DID NOT RESULT IN DEATH OR SERIOUS INJURY AND DOES NOT HAVE THE LIKELIHOOD TO RESULT IN DEATH OR SERIOUS INJURY TO THE PATIENT. THIS IS BEING REPORTED OUT OF AN ABUNDANCE OF CAUTION AND AS PER GUIDANCE BY AN FDA INSPECTOR WHO ADVISED THAT THE FDA MIGHT BE INTERESTED IN THE DATA FOR TRENDING PURPOSES. B3: THE DATE OF THE EVENT WAS UNKNOWN TO THE CUSTOMER. D4: THE DEVICE COMPRISES OF 4 SETS OF COMPONENTS. THE LOT # FOR THE 4TH ITEM, THE STRAPS, IS # S061622. THE EXPIRY DATES ARE AS FOLLOWS: EMATD12010 =2023-09-15, EMABN2 =2025-05-30, EMABP = 2025-05-30, EMAST21YM =2025-06-16.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT HAD A REACTION TO THE EMA (ELASTIC MANDIBULAR ADVANCEMENT) THAT WAS ISSUED. IT IS UNCLEAR WHEN THE PATIENT RECEIVED THE DEVICE, WHEN THE PATIENT FIRST USED THE DEVICE, OR WHEN THE REACTION OCCURRED OR RESOLVED. HOWEVER, IT IS NOTED THAT THE PATIENT EXPERIENCED BURNING SENSATION ON THE TONGUE AND BUCCAL MUCOSA. THE DEVICE WAS WORN FOR 2-3 WEEKS (EXACT DATES UNKNOWN). THE SYMPTOMS WENT AWAY AFTER A FEW DAYS OF NON-USE (EXACT DATE UNKNOWN).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1248011 EMA SLEEP DEVICE LRK THE MYERSON COMPANY LIMITED EMATD12010,EMABN2,EMABP,EMAST21YM TD091522 BN2B053022 BP053022

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown