TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1869-2023)

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 100180070

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1869-2023

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: 970 units

Code Information:

UDI/DI 14026704340511, Batch Numbers: 18HG40, 18LG33, 19CT36, 19FT19, 19GT46, 19LT31, KME21A2555, KME22H2313, KME22K1045

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated