BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NATURAL KNEE HIGH TIBIAL LOCATING NEEDLE

    MDR report key: 2080657 · Received April 26, 2011

    Report

    Report Number
    1822565-2011-01034
    Event Type
    Injury
    Date Received
    April 26, 2011
    Date of Event
    March 29, 2011
    Report Date
    March 29, 2011
    Manufacturer
    ZIMMER, INC.
    Product Code
    HAW
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    INFO WAS RECEIVED FROM A FOREIGN SOURCE WHO IS NOT REQUIRED TO COMPLETE FORM 3500A. THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHEN THE NURSE GRABBED THE TRAY TO TAKE IT OUT OF THE FLIGHT CASE, SHE PRICKED HER FINGER ON A LOOSE NEEDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NATURAL KNEE HIGH TIBIAL LOCATING NEEDLE KNEE INSTRUMENT HAW ZIMMER, INC. 61510831

    Patients

    Seq Age Sex Outcome Treatment
    1 Other