TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1945-2023)

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 111780060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1945-2023

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: 16570 units

Code Information:

UDI/DI 14026704341082, Batch Numbers: 18FG12, 18FG23, 18GG03, 18GT26, 18HG24, 18JG14, 18KG08, 18KG22, 18LG31, 19AG09, 19AG11, 19AG21, 19DT42, 19ET34, 19FT18, 19GT44, 19HT66, 19JT01, 19JT20, 19KT17, 19LT04, 19LT08, 19LT31, 19LT32, 20AT09, 20CT23, 20DT29, KME20L1712, KME20M0352

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated