TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1958-2023)

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 112080050

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1958-2023

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: 1750 units

Code Information:

UDI/DI 14026704341266, Batch Numbers: 18FG07, 18JG33, 18JG36, 18LT16, 19CT26, 19KT38, 19LT07, 20AT41, 20CT13, 20ET17, KME20K1512, KME22B0593, KME22E2347, KME22H1178, KME22H3021

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated