BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CARTIVA

    MDR report key: 13606152 · Received February 25, 2022

    Report

    Report Number
    3009351194-2022-00005
    Event Type
    Injury
    Date Received
    February 25, 2022
    Date of Event
    August 20, 2008
    Report Date
    January 4, 2021
    Manufacturer
    CARTIVA
    Product Code
    PNW
    PMA / PMN Number
    P150017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THE PRODUCT WAS NOT RETURNED THEREFORE, PRODUCT ANALYSIS CANNOT BE PERFORMED. THE PRODUCT LOT NUMBER WAS PROVIDED AND THE DEVICE HISTORY RECORD WAS REVIEWED FOR THE COMPLAINT DEVICE. ON NOVEMBER 10TH, 2020 STRYKER TRAUMA AND EXTREMITIES ACQUIRED CARTIVA, WRIGHT MEDICAL, TORNIER INC. AND TORNIER SAS. AN EFFORT WAS MADE TO ALIGN THE ACQUIRED ENTITY COMPLAINT FILES WITH STRYKER'S POLICIES AND PROCEDURES. STRYKER HAS PERFORMED RETROSPECTIVE REVIEW OF COMPLAINTS AND THE REPORTABILITY DECISION WAS REVISED TO REPORT THIS INCIDENT UNDER THE MDR/VIGILANCE PROCESS.

    Description of Event or Problem · 0

    IMPLANT DISLOCATED (LOOSENED).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2359337 CARTIVA PROSTESIS, METATARSOPHALANGEAL JOINT CARTILAGE REPLACEMENT IMPLANT PNW CARTIVA CAR-10 102406001

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Male Other