BEUDAMED
    FDA Adverse Event Summary report: N

    L PLATE LEFT LARGE 2.0 LACTOSORB SYSTEM

    MDR report key: 1984084 · Received February 10, 2011

    Report

    Report Number
    1032347-2011-00016
    Date Received
    February 10, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 30, 2011
    Manufacturer
    BIOMET MICROFIXATION
    Product Code
    HRS
    PMA / PMN Number
    K955729
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    REVIEW OF DEVICE HISTORY RECORDS SHOW THAT LOT RELEASED WITH NO RECORDED ANOMALY OR DEVIATION. THE WARNINGS IN THE PACKAGE INSERT STATE THIS TYPE OF EVENT CAN OCCUR. THE USER FACILITY IS FOREIGN; THEREFORE A FACILITY MEDWATCH REPORT WILL NOT BE AVAILABLE. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A VALID CONCLUSION ABOUT THE CAUSE OF THIS EVENT. IF ADDITIONAL INFORMATION IS OBTAINED THAT ADDS VALUE TO THE RELEVANT CONTENT OF THIS REPORT AND/OR A CONCLUSION CAN BE DRAWN, A FOLLOW-UP REPORT WILL BE SENT. PLATE AND SCREWS WERE EXPLANTED IN THE SAME SURGERY, SEE MDR 1032347-2011-00015 ALSO.

    Description of Event or Problem · 1

    IT WAS REPORTED THE PATIENT HAD LACTOSORB PLATES AND SCREWS IMPLANTED ON (B)(6) 2010 FOR FRACTURE OF THE LEFT CHEEK BONE. ON (B)(6) 2011 THE DOCTOR FOUND THAT THERE WAS PUS AROUND THE MAXILLARY AIR SINUS AND DECIDED TO REMOVE THE IMPLANTS DUE TO THE DISCHARGE OF PUS. THE REMOVAL OCCURRED ON (B)(6) 2011.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 L PLATE LEFT LARGE 2.0 LACTOSORB SYSTEM BONE PLATE HRS BIOMET MICROFIXATION 635290

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization