TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1926-2023)

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:

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1926-2023

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: 5990 units

Code Information:

UDI/DI 14026704340627, Batch Numbers: 19ET31, 19FT28, 19GT08, 19GT31, 19GT35, 19GT48, 19HT05, 19HT32, 19HT60, 19IT38, 20DT09, 20DT24, 20ET03, 20FT55, 20GT37

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated