BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TELEFLEX MEDICALS PILLING WECKSORB NEUROSPONGES

    MDR report key: 23148886 · Received September 25, 2025

    Report

    Report Number
    MW5176611
    Event Type
    Malfunction
    Date Received
    September 25, 2025
    Date of Event
    May 7, 2025
    Report Date
    September 21, 2025
    Manufacturer
    TELEFLEX MEDICAL LLC
    Product Code
    MDM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    DURING DISCECTOMY SURGERY, WHEN SALINE ADDED TO PATTIES AND WHEN IT WAS USED IT STARTED TO SPREAD AND PULL APART.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    302918 TELEFLEX MEDICALS PILLING WECKSORB NEUROSPONGES INSTRUMENT, MANUAL, SURGICAL, GENERAL USE MDM TELEFLEX MEDICAL LLC REF 200106 24K2826

    Patients

    Seq Age Sex Outcome Treatment
    1 15 YR Male