TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1835-2023)

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 170090

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1835-2023

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: 1460 units

Code Information:

UDI/DI 4026704319619, Batch Numbers: 18FG09, 18HG27, 18IG12, 18LG18, 19GT52, 19GT65, 19HT35, 20AT25, KME20L0625, KME21E1232, KME22E2491, KME22E2912

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated