BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KAHOOK DUAL BLADE GLIDE

    MDR report key: 24188644 · Received January 27, 2026

    Report

    Report Number
    1000125279-2026-00001
    Event Type
    Injury
    Date Received
    January 27, 2026
    Date of Event
    December 30, 2025
    Report Date
    January 26, 2026
    Manufacturer
    NEW WORLD MEDICAL, INC.
    Product Code
    QUQ
    PMA / PMN Number
    K220891
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    501

    Narratives

    Additional Manufacturer Narrative · 0

    THE DEVICE HISTORY RECORD (DHR) COULD NOT BE REVIEWED, AS NO SPECIFIC SERIAL OR LOT INFORMATION WAS AVAILABLE. THE PRODUCT WAS MANUFACTURED, TESTED, AND RELEASED IN ACCORDANCE WITH VALIDATED PROCEDURES. AS THE DEVICE IS NOT AVAILABLE FOR RETURN, NO DEVICE MALFUNCTION COULD BE CONFIRMED.

    Description of Event or Problem · 0

    DR. PERFORMED A KDB GLIDE AND PATIENT INCURRED MILD, CONTROLLED HYPHEMA (B)(6) 2025.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    247488 KAHOOK DUAL BLADE GLIDE GONIOTOMY BLADE QUQ NEW WORLD MEDICAL, INC. GLIDE

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention