TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1843-2023)

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:

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1843-2023

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: 2940 units

Code Information:

UDI/DI 14026704644930, Batch Numbers: 18JG21, 18KG18, 19AG09, 19AG37, 19CT32, 19DT33, 19ET38, 19ET77, 19GT45, 19IT54, 20DT29, 20ET56, KME20K0157, KME20L1845, KME20L1846, KME21A0892, KME21B1697, KME21J0153, KME22B1390, KME22B2161, KME22C3335, KME22C3453, KME22F1351, KME22F2419

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated