TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1937-2023)

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 100382055

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1937-2023

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: 7800 units

Code Information:

UDI/DI 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12, 18KG10, 19AG05, 19AT23, 19BG10, 19BG21, 19BG26, 19BT08, 20CT47, 20DT01, 20GG45, 20GT40, KME20H0294, KME20H3036, KME20J0600, KME20J2166, KME20K1116, KME20K1206, KME20K3277, KME20L1040, KME20L1224, KME22F2548

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated