TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1866-2023)

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 100180055

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1866-2023

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: 3309 units

Code Information:

UDI/DI 14026704340481, Batch Numbers: 18IG24, 18JG36, 18LG33, 19AG11, 19AG21, 19DT06, 19ET58, 19FT22, 19FT49, 19HT04, 19HT34, 19HT80, 19IT43, 19JT02, 20AT49, 20BT53, 20CT24, 20DT24, 20GG27, KME20K2673, KME20M0950, KME21A0310, KME21B0602, KME22F0738

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated