TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1956-2023)

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 Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1956-2023

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: 35513 units

Code Information:

UDI/DI 14026704341228, Batch Numbers: 18GG17, 18GG25, 18GT32, 18HG19, 18IG16, 18JG13, 18JG21, 18KG01, 18LG12, 18LG15, 18LG30, 19AG15, 19AG25, 19AG29, 19BG03, 19CT56, 19GT17, 19HT02, 19HT31, 19HT68, 19HT69, 19IT19, 19JT11, 19JT35, 19KT02, 19LT21, 20AT22, 20BG11, 20CT11, 20DT22, 20DT35, 20FT64, 20FT68, 20GT34, 20GT49, KME20H0436, KME20H2683, KME20M0445, KME20M2650, KME21A2042, KME21A2083, KME21A2187, KME21A2929, KME21B0718, KME21B1715, KME21B1946, KME21C0552, KME21C1043, KME21C1044, KME21C1910, KME21C1912, KME21F1682, KME21F1864, KME21K1635, KME21M0798, KME21M2432, KME22A0810, KME22A2177, KME22A2883, KME22A2924, KME22A3263, KME22B2796, KME22C0042, KME22C0206, KME22C0505, KME22D2264, KME22D3154, KME22E1996, KME22E2224, KME22E2513, KME22F0202, KME22H0792, KME22H1588, KME22H2923, KME22J1124, KME22J2482, KME22J3020

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated