BEUDAMED
    FDA Adverse Event Injury Summary report: N

    15" LONG HANDLE REVERSE ANGLED CURETTE

    MDR report key: 21264792 · Received January 29, 2025

    Report

    Report Number
    21264792
    Event Type
    Injury
    Date Received
    January 29, 2025
    Date of Event
    November 5, 2024
    Report Date
    January 7, 2025
    Manufacturer
    LIFE INSTRUMENTS
    Product Code
    HTF
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CO, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    CURETTE FROM RONGEUR TRAY BROKE IN HALF AND CAUSED A DURAL TEAR. CURETTE #: 710-1505-2 11-15M. BROKEN INSTRUMENT REMOVED AND TAKEN TO RISK OFFICE. THE INJURY WAS REPAIRED BY THE SURGEON. CASE COMPLETED AND PATIENT SENT TO RECOVERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1954572 15" LONG HANDLE REVERSE ANGLED CURETTE CURETTE HTF LIFE INSTRUMENTS 710-1505-2

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Required Intervention| O