BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRODIGY LG STAT LNG RT 15.0MM

    MDR report key: 3040178 · Received April 8, 2013

    Report

    Report Number
    1818910-2013-15007
    Event Type
    Injury
    Date Received
    April 8, 2013
    Date of Event
    March 22, 2001
    Report Date
    March 15, 2013
    Manufacturer
    DEPUY ORTHOPAEDICS, INC. 1818910
    Product Code
    LPH
    PMA / PMN Number
    PK000207
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    UPDATED:THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT AND LOT COMBINATION SINCE ITS RELEASE FOR DISTRIBUTION. REQUESTS FOR ADDITIONAL INVESTIGATIONAL INPUTS WERE MADE IN ACCORDANCE WITH WI-7915 APPENDIX A; REV. D. NO ADDITIONAL INFORMATION WAS OBTAINED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT. BASED ON THE INABILITY TO DETERMINE A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED.DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT OR ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.

    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.

    Description of Event or Problem · 1

    CLINICAL REPORT STATES THE PATIENT HAD AN INTRAOPERATIVE COMPLICATION OF A FEMORAL BONE FRACTURE TREATED WITH DALL-MILES CABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    143139 PRODIGY LG STAT LNG RT 15.0MM STEM LPH DEPUY ORTHOPAEDICS, INC. 1818910 VF1AR1014

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Required Intervention