TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1864-2023)

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 uncuffed/plain - Murphy, REF 100180045

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1864-2023

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: 4155 units

Code Information:

UDI/DI 14026704340467, Batch Numbers: 18GT26, 18KG10, 18LG06, 19AG11, 19AG21, 19CT69, 19DT06, 19FT29, 19FT49, 19GT43, 19HT66, 19JT55, 19KT17, 19LT08, 19LT32, 20AT49, 20BT53, 20DT15, 20ET04, 20GG27, KME20H2636, KME20K1812, KME20K2573, KME21L2619, KME21M1773, KME22E2900, KME22G0347, KME22J3224, KME22K0489

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated