TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1883-2023)

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 112080100

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1883-2023

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: 690 units

Code Information:

UDI/DI 14026704341266, Batch Numbers: 18FT26, 18IT18, 18KG10, 19CG03, 19IT31, 20BT13, 20DT18, 20GT57, KME22C0947

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated