BEUDAMED
    FDA Enforcement Class I Ongoing

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

    Recall: Z-1867-2023 · Reported July 5, 2023

    Enforcement

    Recall Number
    Z-1867-2023
    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 100180060

    Reason

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

    Code Info

    UDI/DI 14026704340498, Batch Numbers: 18KG08, 18LG33, 19AG21, 19BG12, 19ET12, 19FT19, 19HT34, 19IT12, 19IT43, 19LT32, 20AT49, 20DT15, 20GG27, KME20K1813, KME20L2063, KME20M1586, KME21A2393, KME21C3189, KME22D3370, KME22F2673

    Distribution

    US Nationwide distribution including Puerto Rico.

    Quantity

    2714 units