TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1899-2023)

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 112480045

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1899-2023

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: 30391 units

Code Information:

UDI/DI 14026704341532, Batch Numbers: 18FG02, 18FG14, 18GT16, 18HG37, 18IG13, 18KG34, 18LG03, 19AG04, 19AG08, 19AG23, 19AG38, 19BG35, 19CG05, 19DT09, 19FT12, 19IT38, 19JT19, 19JT21, 19KT58, 19LT09, 19LT27, 20AT06, 20BG15, 20CT07, 20CT12, 20CT54, 20DT01, 20DT09, 20ET30, 20FT58, 20GT22, KME20H0774, KME20J0792, KME20J2687, KME20M0861, KME20M1576, KME20M1925, KME20M1926, KME20M3207, KME21A0769, KME21B0450, KME21C0314, KME21C1807, KME21K1189, KME21K1920, KME21M1895, KME21M2015, KME21M2776, KME21M3038, KME22B2939, KME22C0808, KME22C0928, KME22D0939, KME22D0940, KME22D1836, KME22D2309, KME22F0391, KME22F1537, KME22F2459, KME22F2526, KME22G1183, KME22H0051, KME22H3521, KME22J2886, KME22K1019, KME22M2104, KME23A1068, KME23A1487, KME23A2313

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated