BEUDAMED
    FDA Adverse Event Injury Summary report: N

    C-SECTION TRAY PACK

    MDR report key: 23407145 · Received October 28, 2025

    Report

    Report Number
    1423395-2025-00180
    Event Type
    Injury
    Date Received
    October 28, 2025
    Date of Event
    October 2, 2025
    Report Date
    October 28, 2025
    Manufacturer
    MEDLINE INDUSTRIES, LP
    Product Code
    LRO
    UDI-DI
    10198459044021
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    RI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    ACCORDING TO THE FACILITY, THE "DR. WAS ELECTROCUTED DURING C-SECTION PROCEDURE. CURRENTLY UNSURE WHAT CAUSED THE INCIDENT, BUT IT MAY HAVE BEEN ITEM 102589; EVACUATOR SMOKE VL HLSTR." NO ADDITIONAL INFORMATION AT THIS TIME. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT CAUSED OR CONTRIBUTED TO SERIOUS INJURY REQUIRING MEDICAL INTERVENTION, THEREFORE, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED. HEALTH EFFECT (E): ELECTROCUTION.

    Description of Event or Problem · 0

    ACCORDING TO THE FACILITY, THE "DR. WAS ELECTROCUTED DURING C-SECTION PROCEDURE. CURRENTLY UNSURE WHAT CAUSED THE INCIDENT, BUT IT MAY HAVE BEEN ITEM 102589; EVACUATOR SMOKE VL HLSTR."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1840676 C-SECTION TRAY PACK LRO MEDLINE INDUSTRIES, LP 25GBV990 10198459044021

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other