TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1960-2023)

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 112080065

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1960-2023

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: 6710 units

Code Information:

UDI/DI 14026704341266, Batch Numbers: 18GT07, 18HG20, 18IG16, 18IG22, 18JG13, 19AT23, 19CT64, 19ET12, 19ET31, 19HT69, 19LT47, 20AT41, 20BT13, 20DT40, 20GT05, KME22A2193, KME22A2546, KME22B2739, KME22C2271, KME22E0189

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated