TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1829-2023)

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 170060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1829-2023

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: 9400 units

Code Information:

UDI/DI 4026704319558, Batch numbers: 18GG31, 18HG22, 18HG32, 18HG35, 18IG09, 18IG24, 18IG27, 18JG17, 18LG12, 19AG37, 19BG12, 19CT49, 19DT15, 19DT20, 19ET22, 19ET38, 19ET77, 19FT18, 19IT14, 19IT25, 19JT42, 20DT29, 20ET04, 20FT34, 20FT54, 20GG41, KME20H1653, KME20J1236, KME20J1237, KME20L1487, KME20L2379, KME20M0494, KME21A0384, KME21A1482, KME21C0293, KME21E1411, KME21G0757, KME21G2208, KME21G2209, KME21K0548, KME21K0549, KME21L0444, KME21M1392, KME22A1512, KME22A1513, KME22B1392

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated