BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    V. MUELLER

    MDR report key: 19180492 · Received April 25, 2024

    Report

    Report Number
    19180492
    Event Type
    Malfunction
    Date Received
    April 25, 2024
    Date of Event
    February 20, 2024
    Report Date
    April 10, 2024
    Manufacturer
    CAREFUSION 2200, INC
    Product Code
    JYG
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    DURING AN OPERATIVE PROCEDURE, THE CURETTE BROKE DURING USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1605980 V. MUELLER CURETTE, EAR JYG CAREFUSION 2200, INC AU5600 C21XSF

    Patients

    Seq Age Sex Outcome Treatment
    1 1 DA Male