TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1837-2023)

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:

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1837-2023

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: 14160 units

Code Information:

UDI/DI 14026704644879, Batch Numbers: 18JG23, 18JG26, 18JG34, 18KG26, 18LG05, 19AG18, 19AG21, 19AG24, 19AG37, 19BG01, 19BG04, 19BG07, 19BG12, 19BG16, 19CT58, 19CT71, 19DT06, 19DT20, 19ET77, 19FT14, KME20H0975, KME20H0976, KME20J0324, KME20K0771, KME20K2545, KME20K2568, KME20L0627, KME21A1886, KME21B1671, KME21B2506, KME21C2475, KME21D0447, KME21K1723, KME22A0056, KME22B0179, KME22B0180, KME22B0181, KME22B0464, KME22C2255, KME22C2256, KME22D1638, KME22D1639, KME22D1788, KME22E1489, KME22F1500, KME22F1669, KME22F1670, KME22G3099, KME22H3107, KME22H3275, KME22J2354, KME22J2355, KME22J2356, KME23A2360

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated