BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DUR UNI US POL TIB 8MM MD L M

    MDR report key: 274674 · Received April 19, 2000

    Report

    Report Number
    9610726-2000-00021
    Event Type
    Injury
    Date Received
    April 19, 2000
    Date of Event
    March 17, 2000
    Report Date
    April 19, 2000
    Manufacturer
    HOWMEDICA INC.
    Product Code
    JWH
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    KNEE REVISION HAS BEEN REPORTED DUE TO WEAR OF TIBIAL INSERT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DUR UNI US POL TIB 8MM MD L M IMPLANT JWH HOWMEDICA INC. NA DC22

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Required Intervention