BEUDAMED
    FDA Enforcement Class I Ongoing

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

    Recall: Z-1870-2023 · Reported July 5, 2023

    Enforcement

    Recall Number
    Z-1870-2023
    Event ID
    92373
    Classification
    Class I
    Status
    Ongoing
    Product Type
    Devices
    Firm
    TELEFLEX LLC
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    July 5, 2023
    Initiation Date
    May 25, 2023
    Classification Date
    June 29, 2023
    Address
    3015 Carrington Mill Blvd, N/A, Morrisville, NC, 27560-5437, United States

    Description

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

    Reason

    Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

    Code Info

    UDI/DI 14026704340528, Batch Numbers: 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753

    Distribution

    US Nationwide distribution including Puerto Rico.

    Quantity

    2874 units