BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6961180

    MDR report key: 6961180 · Received October 19, 2017

    Report

    Report Number
    6961180
    Event Type
    Malfunction
    Date Received
    October 19, 2017
    Date of Event
    October 6, 2017
    Report Date
    October 9, 2017
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DOCTOR WAS DOING A TOTAL KNEE ARTHROPLASTY WHEN HE TURNED AROUND AND SAID THAT THE BLADE THAT HE WAS USING WAS NOT SHARP AND THAT HE FELT THAT IT WAS A REFURBISHED BLADE. THE DOCTOR WAS GIVEN A NEW SHARP BLADE.

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR