TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1955-2023)

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 111781065

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1955-2023

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: 37890 units

Code Information:

UDI/DI 14026704341211, Batch Numbers: 18FG20, 18FG31, 18GG17, 18HG21, 18IG16, 18IG30, 18JG16, 18JG20, 18KG01, 18LG30, 19AG01, 19AG25, 19AG29, 19BG18, 19CG02, 19DT35, 19DT46, 19ET36, 19FT01, 19FT02, 19FT45, 19GT63, 19HT55, 19HT68, 19IT53, 19KT14, 19KT46, 19LT17, 19LT21, 20AT22, 20BT01, 20CT11, 20CT32, 20DT19, 20ET39, 20FT18, 20FT64, KME20H0432, KME20H2681, KME20L2673, KME20M1288, KME20M2831, KME20M2957, KME21A2081, KME21A2935, KME21B0719, KME21B1201, KME21B1825, KME21B1947, KME21C0646, KME21C1045, KME21C3350, KME21D1229, KME21E0011, KME21F0146, KME21K1657, KME21K1658, KME21K1713, KME21K1748, KME21L2302, KME21L2792, KME21L2886, KME22A1379, KME22A1884, KME22A1885, KME22A2922, KME22C0332, KME22C0413, KME22C1125, KME22C1127, KME22C1581, KME22C2971, KME22D0261, KME22D1843, KME22D3133, KME22E0948, KME22E0949, KME22F0366, KME22F0988, KME22F3121, KME22G0692, KME22G1335, KME22G3063, KME22H0521, KME22H1633, KME22H3274, KME22J0144, KME22J1123, KME22J2413, KME22J2479, KME22K0090

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated