TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1927-2023)

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 - Magill, REF 100380035

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1927-2023

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: 2860 units

Code Information:

UDI/DI 14026704340634, Batch Numbers: 18HG08, 18IG13, 18JG35, 18LG31, 19BG15, 19CT16, 19ET31, 19HT07, 19HT79, 19LT28, 20GT37, KME20H2590, KME20L0690, KME22D0945, KME22E1145, KME22G2935, KME22J0819, KME22J2900

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated