TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1928-2023)

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 100380040

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1928-2023

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: 3370 units

Code Information:

UDI/DI 14026704340641, Batch Numbers: 19FT28, 19GT04, 19GT51, 19KT13, 19LT28, 20BG15, 20ET03, KME20H2609, KME20J3088, KME20K2749, KME20L0640, KME20M1726, KME20M2538, KME21A0858, KME21M2918, KME22B2857, KME22C3373, KME22D0876

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated