TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1959-2023)

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 112080060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1959-2023

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: 4160 units

Code Information:

UDI/DI 14026704341266, Batch Numbers: 18GG26, 18GT08, 18GT11, 18IG22, 18IT18, 18JG33, 19AG39, 19ET31, 19GT25, 19IT20, 19KT14, 19KT47, 20AT58, 20CT13, 20FT66, KME20J1463, KME21K0521, KME22A2893, KME22B2215, KME22C2044, KME22G2998, KME22J0859

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated