BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 1868660 · Received October 6, 2010

    Report

    Report Number
    9610617-2010-00030
    Event Type
    Other
    Date Received
    October 6, 2010
    Date of Event
    September 3, 2010
    Report Date
    October 1, 2010
    Manufacturer
    KARL STORZ GMBH & CO. KG
    Product Code
    KOG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ALLEGEDLY, FED-X EMPLOYEE WAS JABBED IN THE FINGER BY ONE OF OUR INSTRUMENTS THAT WAS STICKING THROUGH THE BOX; THE INJURY WAS DESCRIBED AS MINOR. THE EMPLOYEE RECEIVED A SHOT FOR TETANUS AND HEPATITIS. THE INSTRUMENT WAS RETURNING TO US FROM A HOSP; THEY PACKED AND SENT IT. I CONFIRMED AND RELAYED INFO TO FED-X THAT THE INSTRUMENTS HAD BEEN CLEANED AND STERILIZED BEFORE BEING SENT VIA FED-X.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ SCISSORS INSERT KOG KARL STORZ GMBH & CO. KG 34310MS

    Patients

    Seq Age Sex Outcome Treatment
    1 Other