BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VNGD PS+ TIB BRG 10X71/75MM

    MDR report key: 18261111 · Received December 4, 2023

    Report

    Report Number
    0001825034-2023-02862
    Event Type
    Injury
    Date Received
    December 4, 2023
    Report Date
    December 27, 2023
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JWH
    PMA / PMN Number
    K113550
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). D10: 183110 - VAN PS OPEN INTL FEM-RT 67.5 - 020610 141213 - BIOMET ILOK PRI TIB TRAY 71MM - 863040 141318 - BIOMET FINNED PRI STM 80X12.5 - 455540 11-150842 - BMET ARCOM AP PAT 3PST 34MM MD - 165150 UNKNOWN - UNKNOWN CEMENT - UNKNOWN CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION AS IT REMAINS IMPLANTED. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2023-02859 0001825034-2023-02860 0001825034-2023-02861 0001825034-2023-02863

    Additional Manufacturer Narrative · 0

    THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. THE DEVICE HISTORY RECORD WAS REVIEWED AND NO DISCREPANCIES RELEVANT TO THE REPORTED EVENT WERE FOUND. PRIMARY OPERATIVE NOTES STATE NO INTRA OPERATIVE COMPLICATIONS. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT TOTAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT HAS HAD ONGOING TREATMENT AND THERAPY AND NOTED THE POSSIBILITY OF A REVISION. NO FURTHER OUTCOMES OR REVISIONS HAVE BEEN REPORTED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.

    Description of Event or Problem · 0

    NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2177289 VNGD PS+ TIB BRG 10X71/75MM PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 101280

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Required Intervention SEE H10.