BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FINE SURGICAL INSTRUMENTS

    MDR report key: 17181087 · Received June 22, 2023

    Report

    Report Number
    17181087
    Event Type
    Malfunction
    Date Received
    June 22, 2023
    Date of Event
    April 27, 2023
    Report Date
    June 6, 2023
    Manufacturer
    FINE SURGICAL INSTRUMENTS, INC.
    Product Code
    HDJ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NV
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    TIP OR CORD CLAMP CUTTER STICK IN CLAMP WHILE ATTEMPTING TO REMOVE. REMOVED, USED A DIFFERENT CORD CLAMP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1012649 FINE SURGICAL INSTRUMENTS SCISSORS, UMBILICAL HDJ FINE SURGICAL INSTRUMENTS, INC. 2922

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown