BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/17 MM L

    MDR report key: 20062235 · Received August 26, 2024

    Report

    Report Number
    3005180920-2024-00659
    Event Type
    Injury
    Date Received
    August 26, 2024
    Date of Event
    July 27, 2024
    Report Date
    August 26, 2024
    Manufacturer
    MEDACTA INTERNATIONAL SA
    Product Code
    JWH
    UDI-DI
    07630030826450
    PMA / PMN Number
    K121416
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    BATCH REVIEW PERFORMED ON 02-AUG-2024. LOT 143365: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 22-JUL-2014. EXPIRATION DATE: 2019-05-31. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN SOLD WITH NO SIMILAR REPORTED EVENT DURING THE PERIOD OF REVIEW.

    Description of Event or Problem · 0

    AT ABOUT 9 YEARS AFTER PRIMARY, THE PATIENT CAME IN DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED A WASHOUT AND REVISED THE LINER. THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    230975 GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/17 MM L KNEE TIBIAL INSERT JWH MEDACTA INTERNATIONAL SA 143365 07630030826450

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention