---
title: "Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135 — FDA record Z-1840-2023 | 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-1840-2023-slick-set-uncuffed-endotracheal-tube-and-stylet-set-oral-nasal-ref-170135/
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 170135 — FDA record Z-1840-2023

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 170135
- **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**: 20662 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1840-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1840-2023%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 14026704647030, Batch Numbers: 18KG03, 18KG07, 18KG18, 18LG22, 19AG18, 19AG21, 19AG24, 19AG37, 19BG04, 19BG12, 19BG40, 19CT49, 19CT58, 19DT06, 19DT20, 19DT38, 19ET22, 19ET28, 19GT45, 19GT59, 19GT65, 19HT05, 19HT35, 19HT61, 19HT66, 19IT54, 19JT22, 19JT29, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT36, 20DT09, 20DT37, 20ET16, 20ET21, 20ET28, KME20G0242, KME20H1846, KME20J0328, KME20J1234, KME20K1629, KME20K2547, KME20K2583, KME20K3590, KME20L0632, KME20L1486, KME20L2401, KME20M0811, KME20M3276, KME20M3277, KME21A1898, KME21A2813, KME21B1686, KME21C0018, KME21D1850, KME21E0464, KME21K1250, KME21L1893, KME21L1894, KME21L2343, KME22A0207, KME22A1510, KME22B0538, KME22B0726, KME22B1029, KME22B2334, KME22C1825, KME22C2261, KME22E2104, KME22E2263, KME22E2264, KME22F2163, KME22F2418, KME22H0050, KME22H0350, KME22H2625, KME22J0996 |

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. They are not inferred from the firm's address.

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 5, 2023
- **Recall initiation date**: May 25, 2023
- **Center classification date**: Jun 29, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. 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-1840-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [TELEFLEX LLC records](https://isitonrecall.com/brand/teleflex-llc/)
