BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PFC C/R FEM CEM LFT SZ5

    MDR report key: 2141293 · Received June 22, 2011

    Report

    Report Number
    1818910-2011-10282
    Event Type
    Injury
    Date Received
    June 22, 2011
    Date of Event
    May 23, 2011
    Report Date
    May 23, 2011
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    JWH
    PMA / PMN Number
    K884796
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

    Additional Manufacturer Narrative · 1

    EXAMINATION OF THE SUBMITTED FEMORAL COMPONENT DID NOT FIND ANY EVIDENCE CONFIRMING DEVICE LOOSENING. BASED ON THE INVESTIGATIONS INABILITY TO FIND EVIDENCE OF DEVICE LOOSENING OR PRODUCT CONTRIBUTION TO THE REPORTED EVENT, A NEED FOR CORRECTIVE ACTION IS NOT INDICATED. BASED ON THE PERFORMED INVESTIGATION, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

    Description of Event or Problem · 1

    THE PATIENT WAS REVISED BECAUSE OF LOOSENING OF THE TIBIAL TRAY AND FEMORAL COMPONENT AT THE CEMENT/IMPLANT INTERFACE. UNKNOWN CEMENT MANUFACTURER. OSTEOLYSIS AND POLYETHYLENE WEAR NOTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PFC C/R FEM CEM LFT SZ5 87 JWH JWH DEPUY ORTHOPAEDICS, INC. NA 022456

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention