BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRATT RECTAL PROBE 73/4 SILVER

    MDR report key: 1981066 · Received November 22, 2010

    Report

    Report Number
    2523190-2010-00015
    Event Type
    Malfunction
    Date Received
    November 22, 2010
    Date of Event
    September 13, 2010
    Report Date
    November 22, 2010
    Product Code
    ITX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRATT RECTAL PROBE 73/4 SILVER NA ITX

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Required Intervention