TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1954-2023)

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 111781060

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1954-2023

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: 43571 units

Code Information:

UDI/DI 14026704341204, Batch Numbers: 18FT39, 18GT32, 18HG19, 18IG10, 18IG16, 18IG30, 18JG35, 18LG15, 18LG30, 19AG15, 19AG25, 19CT33, 19CT36, 19DT35, 19DT46, 19ET34, 19ET69, 19FT01, 19GT13, 19GT17, 19GT63, 19HT68, 19IT01, 19IT53, 19JT15, 19JT35, 19KT41, 19LT21, 19LT36, 20AT22, 20BT02, 20CT32, 20DT35, 20ET34, 20ET39, 20FT18, 20FT64, KME20H0431, KME20L2192, KME20M0306, KME20M1285, KME20M2828, KME20M2905, KME21A1085, KME21A2932, KME21A3056, KME21B0722, KME21B1047, KME21B1628, KME21B2706, KME21C1054, KME21C2465, KME21C3344, KME21D2006, KME21D2007, KME21F1423, KME21J1549, KME21K3004, KME21L1432, KME21L2739, KME21M0028, KME21M0163, KME21M0799, KME21M2429, KME21M2911, KME21M3080, KME22A0809, KME22A1219, KME22B1419, KME22C1123, KME22C1555, KME22C1556, KME22C2192, KME22C2845, KME22C2970, KME22D0540, KME22D1570, KME22D1620, KME22D1841, KME22D2294, KME22D2491, KME22E2435, KME22E2436, KME22E2874, KME22G0208, KME22G0690, KME22G0862, KME22G1268, KME22G2247, KME22G2660, KME22G3252, KME22H1630, KME22H2409, KME22J1083, KME22J2876

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated