TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1871-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1871-2023

Event ID: 92373

Reason for Recall:

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

Status: Ongoing

Product Quantity: 12852 units

Code Information:

UDI/DI 14026704340542, Batch Numbers: 18GG17, 18GG34, 18IG15, 18JG03, 18JG21, 18KG18, 18LG14, 18LG15, 19AG25, 19BG02, 19ET39, 19FT46, 19HT31, 19IT01, 19IT53, 19KT02, 19LT21, 20AT26, 20CT11, 20DT19, 20DT32, KME20J0427, KME20M0303, KME21A2096, KME21A3064, KME21B2620, KME21B2621, KME21C1148, KME21C3436, KME21D0720, KME21D2148, KME21M2369, KME22B0041, KME22B0278, KME22B0588, KME22C0507, KME22D3254, KME22F0607, KME22F2175

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated