TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1940-2023)

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 111780035

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1940-2023

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: 36135 units

Code Information:

UDI/DI 14026704341037, Batch Numbers: 18GG03, 18GG24, 18GT26, 18HG36, 18IG11, 18JG07, 18JG14, 18JG36, 18KG22, 18KG34, 18LG31, 19AG21, 19AG36, 19BG12, 19CG07, 19CT36, 19CT69, 19DT42, 19FT22, 19FT49, 19GT43, 19HT03, 19JT01, 19JT20, 19JT55, 19LT32, 20AT09, 20CT24, 20DT15, 20ET04, 20ET56, 20GG43, 20GT18, KME20H2627, KME20L2489, KME20M0355, KME20M1519, KME21A0965, KME21A2395, KME21B1964, KME21B2528, KME21C0337, KME22A1674, KME22B1172, KME22B1719, KME22C0647, KME22D0114, KME22D2229, KME22E0680, KME22E1094, KME22E2895, KME22E2896, KME22F1454, KME22F1458, KME22F2737, KME22G0575, KME22H0031, KME22H0797, KME22H1789, KME22H2875, KME22H3073, KME22J1158, KME22J1777, KME22K2438, KME22L1579, KME22L1617, KME22L1659, KME22L1725, KME23A2277, KME23A3144, KME23B0437

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated