TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1834-2023)

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 170085

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1834-2023

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: 4370 units

Code Information:

UDI/DI 4026704319602, Batch Numbers: 18FG09, 18GG20, 18GG28, 18HG07, 18JG11, 18KG18, 19AG37, 19CT32, 19DT02, 19ET38, 19ET60, 19HT61, 19HT66, 19IT44, 19KT21, 19KT55, 19LT32, 20AT32, 20BT05, 20BT23, 20CT51, 20GG36, KME20L0398, KME20L2376, KME20M3247, KME21C0298, KME21E1296, KME21K1876, KME21L0573, KME22F0484

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated