BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRESERVATION UNI FEM CEM SZ 3

    MDR report key: 1060574 · Received June 12, 2008

    Report

    Report Number
    1818910-2008-02157
    Event Type
    Injury
    Date Received
    June 12, 2008
    Date of Event
    May 19, 2008
    Report Date
    May 19, 2008
    Manufacturer
    DEPUY - CORK, A DIV OF DEPUY ORTHOPAEDICS
    Product Code
    HRY
    PMA / PMN Number
    K010810
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL WAS NOT POSSIBLE, AS THE PRODS WERE NOT RETURNED. A REVIEW OF THE DEVICE HISTORY RECORDS DID NOT REVEAL ANY ANOMALIES. A SEARCH OF THE COMPLAINT DATABASE DID NOT REVEAL ANY OTHER REPORTS AGAINST THE MFG LOTS. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY CONCLUSIONS ABOUT THE REPORTED POLYETHYLENE WEAR OR DEVICE LOOSENING. NO EVIDENCE WAS FOUND SUGGESTING PROD ERROR WAS A CONTRIBUTING FACTOR AND THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED.

    Description of Event or Problem · 1

    THE PT WAS REVISED BECAUSE OF PAIN, WEAR AND LOOSENING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRESERVATION UNI FEM CEM SZ 3 87HRY HRY DEPUY - CORK, A DIV OF DEPUY ORTHOPAEDICS NA 1913262

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Required Intervention