TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1844-2023)

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 170155

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1844-2023

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: 3310 units

Code Information:

UDI/DI 14026704644947, Batch Numbers: 18JG17, 19AG37, 19CT32, 19ET22, 19ET38, 19ET60, 19IT54, 20AT32, 20CT22, 20DT29, KME20G0385, KME20K2550, KME20L1492, KME20M0813, KME21A2775, KME21B1698, KME21C2646, KME21J0882, KME21J0883, KME22F0239, KME22F0718, KME22F2420, KME22J0254, KME22J0262, KME22K2780

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated