TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1868-2023)

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 100180065

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1868-2023

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: 1570 units

Code Information:

UDI/DI 14026704340504, Batch Numbers: 18JG07, 19AG21, 19BG12, 19HT03, 19HT34, 19JT02, 19LT32, 20AT49, KME20M2642, KME21B0078, KME22D1517, KME22H1720, KME22J0807

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated