BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ZIMMER M/L TAPER FEMORAL STEM

    MDR report key: 3894011 · Received June 10, 2014

    Report

    Report Number
    1822565-2014-00715
    Event Type
    Injury
    Date Received
    June 10, 2014
    Report Date
    June 27, 2013
    Manufacturer
    ZIMMER INC
    Product Code
    MEH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    IT IS REPORTED THE PATIENT IS EXPERIENCING PAIN AND BURSITIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    343408 ZIMMER M/L TAPER FEMORAL STEM MEH ZIMMER INC 61418596

    Patients

    Seq Age Sex Outcome Treatment
    1 Other