BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    WEXLER SURGICAL, INC.

    MDR report key: 25276841 · Received May 26, 2026

    Report

    Report Number
    25276841
    Event Type
    Malfunction
    Date Received
    May 26, 2026
    Date of Event
    February 20, 2026
    Report Date
    May 4, 2026
    Manufacturer
    WEXLER SURGICAL, INC.
    Product Code
    DWS
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AL
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    MD [REDACTED] WAS DOING AN OFF- PUMP CABG [CORONARY ARTERY BYPASS GRAFT] AND THE CORONARY SCISSORS TIP BROKE OFF IN THE PATIENT'S MAMMARY ARTERY. HE WAS ABLE TO RETRIEVE THE TIP OF THE SCISSOR WITHOUT THE PATIENT BEING INJURED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    407785 WEXLER SURGICAL, INC. INSTRUMENTS, SURGICAL, CARDIOVASCULAR DWS WEXLER SURGICAL, INC. SL0741.1F

    Patients

    Seq Age Sex Outcome Treatment
    1