BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 2/14MM

    MDR report key: 12179427 · Received July 16, 2021

    Report

    Report Number
    3005180920-2021-00602
    Event Type
    Injury
    Date Received
    July 16, 2021
    Date of Event
    June 28, 2021
    Report Date
    July 16, 2021
    Manufacturer
    MEDACTA INTERNATIONAL SA
    Product Code
    JWH
    UDI-DI
    07630030816710
    PMA / PMN Number
    K103170
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 1

    BATCH REVIEW PERFORMED ON 08 JULY 2021: LOT 2003156: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 22-JULY-2020. EXPIRATION DATE: 2025-07-09. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN ALREADY SOLD WITHOUT ANY SIMILAR REPORTED EVENT.

    Description of Event or Problem · 1

    1 MONTH AFTER THE PRIMARY SURGERY THE PATIENT CAME IN DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED A WASHOUT AND REVISED THE POLY AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1079079 GMK-REVISION FIXED TIBIAL INSERT SC SIZE 2/14MM KNEE TIBIAL INSERT JWH MEDACTA INTERNATIONAL SA 02.07.0214SCF 2003156 07630030816710

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention