TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1938-2023)

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 uncuffed/plain - Murphy, REF 100382060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1938-2023

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: 5600 units

Code Information:

UDI/DI 14026704340856, Batch Numbers: 18FG02, 18FG28, 18FT08, 18FT33, 18JG15, 18KG23, 18KG39, 20BT17, 20CT07, KME20H1758, KME20H2730, KME21D0828, KME21J0120, KME21J1583, KME22A2339, KME22B0949, KME22B1778, KME22C2310, KME22D1804, KME22F0417, KME22F0556, KME22F1739

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated