TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1935-2023)

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 100382040

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1935-2023

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: 17102 units

Code Information:

UDI/DI 14026704340818, Batch Numbers: 18FG31, 18FG33, 18FT13, 18GG15, 18HG08, 18HG10, 18HG25, 18IG13, 18JG08, 18KG09, 18KG33, 18LG01, 19BG12, 19BG35, 19ET09, 19FT12, 19GT05, 19IT11, 19KT20, 19KT38, 20AT37, 20CT12, 20CT53, 20DT04, 20ET56, 20FT21, 20FT43, 20GT18, KME20G0126, KME20H0286, KME20H1091, KME20H2041, KME20J2613, KME20K0326, KME20K0601, KME20M0209, KME20M1518, KME21B1133, KME21B1830, KME21C1573, KME21C1675, KME21C2245, KME21C3124, KME21D0525, KME21J0629, KME21K0797, KME21L2516, KME21L2526, KME21M0868, KME22C2637, KME22D0032, KME22D0811, KME22D0943, KME22D1009, KME22E0606, KME22E1274, KME22E2288

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated