TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1842-2023)

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 170145

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1842-2023

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: 4320 units

Code Information:

UDI/DI 14026704644923, Batch Numbers: 18JG14, 18LG15, 19AG24, 19BG12, 19BG16, 19CT49, 19IT25, 20BT05, 20CT12, 20CT51, 20DT29, 20GG41, KME20H2929, KME20K1886, KME20K2586, KME20L1488, KME20L2377, KME21A1891, KME21C0019, KME21C1566, KME21C1974, KME21D0445, KME21J1149, KME21M1818, KME21M2952, KME22D1896, KME22E1744

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated