TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1872-2023)

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 uncuffed/plain - Murphy, REF 100181045

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1872-2023

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: 53216 units

Code Information:

UDI/DI 14026704340559, Batch Numbers: 18FG31, 18FT35, 18GG17, 18GG25, 18GG34, 18HG17, 18IG14, 18JG16, 18JG35, 18JG37, 18KG17, 18KG36, 18KG41, 18LG14, 18LG39, 19AG25, 19BG02, 19BG32, 19CG01, 19CG02, 19CT26, 19CT53, 19CT56, 19CT57, 19DT03, 19DT34, 19DT42, 19ET61, 19GT13, 19GT16, 19GT60, 19HT59, 19LT36, 20AT26, 20CT05, 20CT32, KME21C1880, KME21D0722, KME21D1235, KME21D2149, KME21D2150, KME21L2312, KME21M0208, KME21M0957, KME21M0958, KME21M0959, KME21M2377, KME21M2379, KME22B0281, KME22B1307, KME22B1308, KME22B1464, KME22C0411, KME22C2193, KME22D1004, KME22D1005, KME22E1405, KME22E1503, KME22E2767, KME22F0777, KME22F1313, KME22F2624, KME22G0321, KME22G1706, KME22G2273, KME22H0491, KME22H1075, KME22H1324, KME22J0385

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated