BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LEICA RM2155

    MDR report key: 2281221 · Received September 29, 2011

    Report

    Report Number
    1423337-2011-00005
    Event Type
    Injury
    Date Received
    September 29, 2011
    Date of Event
    August 17, 2011
    Report Date
    August 25, 2011
    Manufacturer
    LEICA BIOSYSTEMS, GMBH
    Product Code
    IDL
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CUSTOMER SUSTAINED AN INJURY TO HIS RIGHT INDEX FINGER TIP WHILE USING THE MICROTOME. HE WAS CUT BY THE MICROTOME BLADE. THE CUSTOMER WENT TO THE EMERGENCY ROOM AT HOSPITAL. STITCHES WERE NOT REQUIRED, ONLY A BANDAGE WAS NECESSARY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LEICA RM2155 MICROTOME IDL LEICA BIOSYSTEMS, GMBH RM2155

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention