TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1930-2023)

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 100380050

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1930-2023

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: 4110 units

Code Information:

UDI/DI 14026704340665, Batch Numbers: 18FG05, 18FT26, 18GT27, 18IG06, 18JG20, 18LG03, 18LT24, 19BG30, 19CT50, 19DT17, 19KT21, 19LT51, 20AT26, 20AT41, 20CT43, 20DT13, 20GG27, KME20H2359, KME20K1713, KME20L1811, KME20M2219, KME21A2253, KME21B0984, KME21L0988, KME22D2223, KME22D3339, KME22E0284, KME22F3118, KME22H2816

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated