TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1939-2023)

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 100382065

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1939-2023

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: 2140 units

Code Information:

UDI/DI 14026704340863, Batch Numbers: 18KG25, 19BT19, 19CT22, 19CT39, 19ET06, KME21L2054, KME22A2341, KME22C2640, KME22E2541, KME22F1554, KME22F2582

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated