TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1865-2023)

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 100180050

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1865-2023

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: 4146 units

Code Information:

UDI/DI 14026704340474, Batch Numbers: 18IG24, 18KG10, 18KG22, 18LG06, 18LG33, 19AG21, 19AG36, 19DT06, 19ET12, 19ET58, 19GT44, 19HT04, 19HT66, 19IT12, 19LT32, 20DT14, 20GG27, KME20J1208, KME21B0077, KME21C0441, KME22D3452, KME22F0736, KME22G0655

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated