TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1923-2023)

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:

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1923-2023

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: 8610 units

Code Information:

UDI/DI 14026704340580, Batch Numbers: 18HG21, 18KG41, 18KG43, 18LG15, 19AG01, 19BG33, 19CT33, 19ET39, 19ET40, 19ET61, 19ET65, 20CT32, KME21M2381, KME22A2300, KME22C2820, KME22D1551, KME22D2353, KME22E1009, KME22E1144, KME22E1407, KME22F2205, KME22F3384

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated