TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1833-2023)

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 170080

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1833-2023

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: 18150 units

Code Information:

UDI/DI 4026704319596, Batch Numbers: 18FG09, 18FG20, 18FT32, 18GG05, 18GG08, 18GG14, 18HG07, 18HG12, 18HG22, 18HG27, 18HG35, 18IG02, 18IG09, 18IG15, 18JG04, 18JG06, 18JG14, 18JG26, 18LG12, 18LG18, 19AG13, 19AG24, 19AG27, 19AG31, 19BG01, 19CT41, 19DT38, 19ET38, 19ET45, 19ET50, 19FT24, 19GT59, 19IT06, 19IT25, 19IT54, 19JT42, 19JT49, 19JT57, 19KT25, 19LT04, 20AT14, 20AT25, 20AT32, 20AT37, 20AT53, 20BT05, 20BT47, 20CT05, 20CT12, 20CT27, 20CT36, 20CT51, 20DT09, 20FT44, 20GT25, KME20H0248, KME20H2019, KME20L0396, KME20L1278, KME20L1279, KME20L2830, KME20M0847, KME21A0386, KME21A2800, KME21A2801, KME21B1245, KME21B2156, KME21C0533, KME21D1204, KME21E1287, KME21F1329, KME21J0410, KME21L0274, KME21L0813, KME21L0851, KME22E2351

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated