BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 2973703 · Received February 20, 2013

    Report

    Report Number
    2973703
    Date Received
    February 20, 2013
    Date of Event
    February 12, 2013
    Report Date
    February 19, 2013
    Manufacturer
    AMD RITMED
    Product Code
    KKX
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MT, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    THE OR RECIEVED A BULK OF UNSTERILE BLUE TOWELS WITH STAINING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    74795 * ACCESSORY, OPERATING ROOM KKX AMD RITMED * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *