TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1861-2023)

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 100180030

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1861-2023

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: 3100 units

Code Information:

UDI/DI 14026704340436, Batch Numbers: 18GG26, 18GT26, 18JG14, 19AG21, 19CG07, 19CT69, 19DT42, 19ET34, 19FT29, 19HT04, 19IT43, 19KT17, 19LT08, 20DT15, 20DT24, 20ET56, KME20K1810, KME20M0946, KME20M2783, KME21A2389, KME21B0075, KME21B1923, KME22D1514, KME22F2666, KME22G0172, KME22G1751

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated