BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DUROTIP DISSECTING SCISSORS

    MDR report key: 7142072 · Received December 21, 2017

    Report

    Report Number
    MW5074175
    Event Type
    Injury
    Date Received
    December 21, 2017
    Date of Event
    December 4, 2017
    Report Date
    December 20, 2017
    Manufacturer
    AESCULAP
    Product Code
    HRR
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    A (B)(6) FEMALE PATIENT UNDERWENT LEFT TOTAL HIP REPLACEMENT. DURING PROCEDURE, IT WAS NOTED THAT TWO PIECES OF THE LONG MAYO SCISSORS HAD BROKEN OFF. DIAGNOSTIC IMAGING WAS UTILIZED TO SUCCESSFULLY RETRIEVE BOTH PIECES. REST OF PROCEDURE CONCLUDED UNEVENTFULLY AND PATIENT WAS SUBSEQUENTLY DISCHARGED HOME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    920429 DUROTIP DISSECTING SCISSORS DUROTIP DISSECTING SCISSORS HRR AESCULAP

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Hospitalization| R