TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1847-2023)

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:

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1847-2023

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: 103842 units

Code Information:

UDI/DI 4026704547593, Batch Numbers: 18FG03, 18FG15, 18FG28, 18GG24, 18IG27, 18JG02, 18JG17, 18JG26, 18JG34, 18KG09, 18KG35, 18LG05, 18LG12, 18LG18, 18LG37, 19AG27, 19AG37, 19BG12, 19CT32, 19CT41, 19CT55, 19CT58, 19ET66, 19ET77, 19FT14, 19FT24, 19FT35, 19GT05, 19GT45, 19HT05, 19HT61, 19JT42, 19KT17, 19KT21, 19KT65, 19LT04, 19LT23, 20AT09, 20AT37, 20AT53, 20BT51, 20CT05, 20CT12, 20CT36, 20DT37, 20ET04, 20FT10, 20FT35, 20GT06, KME20H0129, KME20H0906, KME20H1791, KME20H1847, KME20J0848, KME20K1550, KME20L0336, KME20M0492, KME21E1412, KME21G2207, KME21H0839, KME21H0972, KME21H1124, KME21K0660, KME21K1165, KME21L0442, KME21L0443, KME21L1900, KME21L2539, KME21M1391, KME22A1432, KME22B1411, KME22C1068, KME22C2858, KME22D0479, KME22D0482, KME22D0592, KME22D2846

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated