TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1941-2023)

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 111780040

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1941-2023

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: 20042 units

Code Information:

UDI/DI 14026704341044, Batch Numbers: 18FG24, 18GG03, 18GG04, 18GG24, 18GT26, 18HG24, 18JG07, 18KG22, 18KG34, 18LG33, 19AG36, 19BG12, 19CG07, 19CT69, 19DT42, 19ET58, 19FT18, 19GT43, 19GT44, 19JT55, 19KT38, 19LT32, 20AT09, 20AT49, 20BT53, 20DT24, 20ET50, 20FT36, 20FT60, 20GT40, KME21C0405, KME21C1057, KME22C0550, KME22C0648, KME22C1816, KME22C2806, KME22D1073, KME22D2150, KME22E0683, KME22E0684, KME22E2814, KME22E2897, KME22F1760, KME22F2739, KME22G0790, KME22H1304, KME22H2878, KME22J1447, KME22K0482, KME23A1241, KME23A2001, KME23A2181, KME23A2683, KME23A3032

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated