BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    7951125

    MDR report key: 7951125 · Received October 10, 2018

    Report

    Report Number
    7951125
    Event Type
    Malfunction
    Date Received
    October 10, 2018
    Date of Event
    October 1, 2018
    Report Date
    October 2, 2018
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    RI
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    WHILE SURGEON WAS USING VESSEL SEALER. A RECOVERABLE FAULT OCCURRED STATING BLADE WAS EXPOSED. INSTRUMENT REMOVED FROM PATIENT AND PACKAGED TO BRING TO ACM.

    Patients

    Seq Age Sex Outcome Treatment
    1