BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NX3

    MDR report key: 3680024 · Received March 14, 2014

    Report

    Report Number
    2024312-2014-00163
    Event Type
    Injury
    Date Received
    March 14, 2014
    Report Date
    February 12, 2014
    Manufacturer
    KERR CORPORATION
    Product Code
    EMA
    PMA / PMN Number
    K013609
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 1

    ALTHOUGH THE DOCTOR IDENTIFIED FOUR (4) DIFFERENT LOTS ASSOCIATED WITH THE DEBONDING, SHE COULD NOT VERIFY WHICH LOT WAS USED ON EACH PATIENT. THE LOTS INVOLVED IN THE ALLEGED INCIDENTS INCLUDE LOT NUMBERS 4813434, 4855372, 4872984 AND 4950258. THE PATIENT HAD EXPERIENCED A DEBONDING OF A CROWN; HOWEVER, THE DOCTOR COULD NOT RECALL SPECIFIC PATIENT OR INCIDENT DETAILS. TO DATE, THE PATIENT IS DOING FINE. THE PRODUCTS ALLEGED IN THIS INCIDENT WAS NOT RETURNED; THEREFORE, AN 'ADHESIVE STRENGTH' TEST OF THE RETAIN SAMPLES WERE EVALUATED, YIELDING RESULTS WITHIN SPECIFICATIONS. A DHR REVIEW REVEALED THAT THERE WERE NO DEVIATIONS IN THE MANUFACTURING PROCESS. IN ADDITION, NO SIMILAR COMPLAINTS WERE RECEIVED WITH REGARD TO THESE LOTS.

    Description of Event or Problem · 1

    A DOCTOR ALLEGED THAT THREE (3) PATIENTS HAD EXPERIENCED THE DEBONDING OF RESTORATIONS AFTER PLACEMENT USING THE NX3 CEMENT AND THE OPTIBOND XTR PRODUCTS. THIS IS THE THIRD OF THREE (3) REPORTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    153251 NX3 DENTAL CEMENT EMA KERR CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Other| R OPTIBOND XTR