TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1877-2023)

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 Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1877-2023

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: 15810 units

Code Information:

UDI/DI 14026704341112, Batch Numbers: 18FG21, 18FG31, 18GG19, 18HG23, 18HG30, 18IG16, 18IG30, 18JG35, 18KG19, 18KG41, 18LG18, 19AG03, 19BG04, 19BG19, 19CG03, 19CT36, 19DT34, 19FT37, 19GT65, 19HT55, 19IT01, 19IT19, 19JT38, 19LT21, 20AT26, 20BG11, 20CT12, 20DT22, 20ET04, 20ET49, 20FT65, KME20H0627, KME20K0991, KME20K3625, KME20L2680, KME21A1113, KME21A2088, KME21A3085, KME21B0714, KME21B2708, KME21C0596, KME21C1167, KME21L0761, KME21L0859, KME22A1383, KME22B2543, KME22B2906, KME22D0652, KME22D3251, KME22E1151, KME22E1506, KME22G0386, KME22G3151, KME22G3270, KME22H2700, KME22J0257, KME22J1105, KME22J1335, KME22K3101, KME22M1594

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated