TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1895-2023)

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:

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480025

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1895-2023

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: 66244 units

Code Information:

UDI/DI 14026704341495, Batch Numbers: 18FG31, 18GT32, 18IG03, 18IG29, 18KG08, 18LG03, 19AG08, 19AG38, 19BG12, 19BG35, 19DT13, 19DT36, 19ET51, 19FT12, 19FT28, 19GT02, 19HT05, 19HT79, 19IT59, 19LT08, 19LT31, 20BG15, 20BT01, 20CT07, 20DT24, 20ET53, 20GT38, KME20H2416, KME20H2417, KME20J1068, KME20K2143, KME20K2598, KME20L0449, KME20L1346, KME20M0127, KME20M1797, KME21A0348, KME21B0087, KME21B0465, KME21C0163, KME21C1805, KME21C2447, KME21C2688, KME21C3244, KME21K2877, KME22A1408, KME22A2390, KME22A2545, KME22B0845, KME22B2017, KME22B2848, KME22C2802, KME22E0598, KME22E2130, KME22E2191, KME22G1878, KME22G2593, KME22H0532, KME22H1185, KME22H2178, KME22H2180, KME22J1309, KME22J2321

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated