TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1925-2023)

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 100380025

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1925-2023

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: 3590 units

Code Information:

UDI/DI 14026704340610, Batch Numbers: 19ET51, 19FT29, 19GT05, 19GT35, 19HT79, 19JT51, 19KT06, 19LT28, 20AT05, 20AT37, 20AT54, 20BG15, 20DT24, 20ET03, KME21B0529, KME21C0887, KME21D0327, KME21F0137, KME21K0799, KME21K0800, KME22A2704, KME22C0981, KME22C1568, KME22D0029, KME22H0686, KME22H1360

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated