BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BIOHORIZONS DENTAL IMPLANT

    MDR report key: 14438163 · Received May 19, 2022

    Report

    Report Number
    1060818-2021-15682
    Event Type
    Injury
    Date Received
    May 19, 2022
    Date of Event
    October 11, 2021
    Report Date
    November 10, 2021
    Manufacturer
    BIOHORIZONS IMPLANT SYSTEMS
    Product Code
    DZE
    PMA / PMN Number
    K182070
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THE DETAILS FOR REPORT NUMBER 1060818-2021-15682 WERE PREVIOUSLY SUBMITTED IN REPORT NUMBER 1060818-2021-12028. REPORT NUMBER 1060818-2021-12028 WAS ORIGINALLY REPORTED AS A 2021 3RD QUARTER VOLUNTARY SUMMARY MALFUNCTION REPORT ON 10/31/2021. HOWEVER, DURING THE PREPARATION OF SINGLE MDR EVENTS DATED 10/11/2021, THE REPORT NUMBER ENDING IN 12028 WAS OVERWRITTEN IN ERROR. THE SINGLE MDR EVENT FOR COMPLAINT (B)(4) SHOULD HAVE NOT BEEN ASSIGNED 1060818-2021-12028 BECAUSE 1060818-2021-12028 HAD ALREADY BEEN USED AND TRANSMITTED. . THEREFORE, THIS SUBMISSION OF 1060818-2021-15682 IS TO CORRECT THE DOUBLE USAGE OF 1060818-2021-12028. REPORT NUMBER 1060818-2021-15682 CREATES THE STAND-ALONE MDR EVENT FOR (B)(4) WHICH WILL ALLOW FOR THE CORRECTION TO 1060818-2021-12028 TO OCCUR. MFR REPORT NUMBER 1060818-2021-12028 WILL BE UPDATED TO ITS ORIGINAL STATE FOR THE 2021 3RD QUARTER VOLUNTARY SUMMARY MALFUNCTION REPORT ASSOCIATED WITH A LOOSE ABUTMENT.

    Description of Event or Problem · 0

    IMPLANT REMOVED DUE TO SURGICAL PREFERENCE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    293926 BIOHORIZONS DENTAL IMPLANT DENTAL IMPLANT DZE BIOHORIZONS IMPLANT SYSTEMS TIM8010 2100221

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Required Intervention