TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1932-2023)

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 100380060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1932-2023

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: 1110 units

Code Information:

UDI/DI 14026704340689, Batch Numbers: 18FG31, 19BT11, 19ET72, 19JT30, 20AT13, 20BT13, 20DT13, KME21D0600, KME21J0790, KME22A0448, KME22D1803

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated