TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1893-2023)

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 Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1893-2023

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: 18620 units

Code Information:

UDI/DI 14026704341471, Batch Numbers: 18HG08, 18HT04, 18IG29, 18IT04, 18JT16, 18KG37, 18KT27, 18LT16, 19BG02, 19CG02, 19CT04, 19CT72, 19GT25, 19HT19, 19HT47, 19JT05, 19KT55, 19LT08, 20AT13, 20CT02, 20CT29, 20DT32, 20GT23, 20GT44, KME20H1486, KME20J1899, KME20K2166, KME20L1592, KME20L2462, KME20L2557, KME20M2115, KME20M2198, KME21A2346, KME21E1393, KME21K1818, KME22B1259, KME22B1420, KME22B1854, KME22C0677, KME22C0713, KME22C0844, KME22C1612, KME22C2606, KME22C2757, KME22D1593, KME22D1778, KME22E1285, KME22E2362, KME22F1401, KME22F2452, KME23A0557, KME23A0763

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated