BEUDAMED
    FDA Adverse Event Injury Summary report: N

    COONRAD/MORREY HUMERAL ASSEMBLY

    MDR report key: 2780657 · Received October 5, 2012

    Report

    Report Number
    1822565-2012-02043
    Event Type
    Injury
    Date Received
    October 5, 2012
    Date of Event
    September 7, 2012
    Report Date
    September 7, 2012
    Manufacturer
    ZIMMER, INC.
    Product Code
    JDC
    Adverse Event
    Yes
    Product Problem
    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 THAT THE PT WAS EXPERIENCING PAIN. UPON X-RAY IT WAS NOTED THAT THE PIN FRACTURED. A REVISION SURGERY WAS PERFORMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COONRAD/MORREY HUMERAL ASSEMBLY JDC ZIMMER, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 91 YR Required Intervention