--- title: "Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130 — FDA record Z-1839-2023 | Is It on Recall" description: "Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products." url: https://isitonrecall.com/recall/fda-device-z-1839-2023-slick-set-uncuffed-endotracheal-tube-and-stylet-set-oral-nasal-ref-170130/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130 — FDA record Z-1839-2023 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date May 25, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130 - **Reason**: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. - **Classification**: Class I - **Recalling firm**: TELEFLEX LLC - **Quantity**: 22400 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1839-2023 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1839-2023%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | UDI/DI 14026704644893, Batch Numbers: 18JG09, 18JG26, 18JG34, 18JG37, 18KG18, 18KG23, 18LG02, 18LG22, 19AG09, 19AG21, 19AG37, 19BG04, 19BG07, 19BG21, 19BG40, 19CT49, 19CT71, 19DT33, 19ET22, 19ET28, 19ET54, 19ET60, 19ET72, 19ET77, 19FT24, 19GT59, 19GT65, 19HT35, 19HT66, 19IT25, 19JT22, 19JT29, 20AT53, 20BT23, 20BT27, 20BT47, 20CT12, 20CT36, 20CT51, 20DT09, 20DT37, 20ET16, 20ET28, 20GT06, KME20H2016, KME20J0326, KME20K0155, KME20K0156, KME20K1885, KME20K2582, KME20K3586, KME20L1485, KME20L1836, KME20L1837, KME20L2400, KME20M0812, KME21A1895, KME21A1896, KME21A2805, KME21A2806, KME21B0578, KME21B1677, KME21C0532, KME21C0534, KME21C2645, KME21C3512, KME21C3513, KME21D1023, KME21D1429, KME21J1143, KME21J1407, KME21J1408, KME21L2341, KME21L2342, KME21M0030, KME22B2145, KME22C0914, KME22C1231, KME22C1232, KME22C1823, KME22C2258, KME22C2260, KME22C3451, KME22E1030, KME22F0301, KME22G0908, KME22G0909, KME22H0667, KME22J0698, KME22K0017, KME22K0919, KME22K0920, KME22K3076 | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution US Nationwide distribution including Puerto Rico. States below are derived from the distribution text, including nationwide wording. 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These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1839-2023%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [TELEFLEX LLC records](https://isitonrecall.com/brand/teleflex-llc/)