TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1881-2023)

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 Magill, High Volume, Low Pressure Cuff, REF 112080055

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1881-2023

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: 2520 units

Code Information:

UDI/DI 14026704341266, Batch Numbers: 18FG02, 18IG29, 18KG28, 19AG39, 19BG02, 19CT64, 19GT31, 19IT33, 20DT18, KME20G0435, KME20K2579, KME21K0764, KME21K1278, KME22B0079, KME22B0080, KME22E2802, KME22H2250

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated