TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1874-2023)

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 uncuffed/plain - Murphy, REF 100382030

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1874-2023

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: 25160 units

Code Information:

UDI/DI 14026704340795, Batch Numbers: 18FT13, 18GT32, 18HG08, 18HG25, 18IG29, 18JG35, 18KG08, 18LG23, 19AG08, 19AG23, 19AG38, 19BG12, 19BG35, 19CT37, 19CT42, 19DT36, 19ET51, 19FT08, 19GT05, 19GT35, 19IT11, 19IT56, 19KT13, 19LT27, 20AT05, 20BT43, 20CT07, 20DT22, 20ET30, 20FT43, 20FT55, 20GT18, KME20K0276, KME20M3220, KME21A0764, KME21C0890, KME21C1020, KME21C1033, KME21C1572, KME21C2686, KME21D1293, KME21D1448, KME21D1743, KME21D1913, KME21F0962, KME22A2454, KME22C1763, KME22D2425, KME22D2823, KME22E0291, KME22E0560, KME22E2506, KME22E2684, KME22E2925, KME22F1606, KME22J1478, KME22K0878, KME22L2920, KME22M0084, KME22M0213

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated