TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1836-2023)

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 Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1836-2023

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: 720 units

Code Information:

UDI/DI 4026704319626, Batch Numbers: 19HT48, 19KT17, 20AT53, 20BT37, KME22E2493, KME22F1387, KME22H0342

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated