TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1924-2023)

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 100181065

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1924-2023

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: 2980 units

Code Information:

UDI/DI 14026704340597, Batch Numbers: 18FT35, 18GG25, 18JG35, 18KG21, 18LG18, 19AG25, 19CT33, 19ET69, 20BT02, 20CT11, KME22B1670, KME22E1010, KME22E1408, KME22H0137, KME22J0202, KME22K2262

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated