TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1901-2023)

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 Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1901-2023

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: 2382 units

Code Information:

UDI/DI 4026704319657, Batch Numbers: 18GT32, 18HG07, 18HG16, 18HG29, 18HG38, 18IG06, 18IG17, 18IG21, 18IG27

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated