---
title: "Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070 — FDA record Z-1831-2023 | 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-1831-2023-slick-set-cuffed-endotracheal-tube-and-stylet-set-oral-nasal-ref-170070/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070 — FDA record Z-1831-2023

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 Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070
- **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**: 50039 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1831-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1831-2023%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 4026704319572, Batch numbers: 18FG09, 18FG15, 18FG17, 18FG20, 18FG21, 18GG10, 18GG28, 18GT32, 18HG07, 18HG16, 18HG35, 18HG38, 18IG09, 18JG02, 18JG17, 18JG37, 18KG23, 18KG35, 18LG05, 18LG12, 18LG18, 19AG13, 19AG31, 19AG34, 19BG04, 19CT17, 19CT41, 19CT49, 19CT55, 19FT24, 19FT41, 19GT05, 19GT10, 19GT52, 19GT59, 19GT65, 19HT40, 19HT66, 19IT44, 19IT54, 19JT22, 19JT42, 19JT57, 19JT64, 19KT30, 19KT41, 19LT04, 19LT17, 20AT14, 20AT25, 20AT44, 20AT53, 20BT05, 20BT23, 20BT47, 20CT05, 20CT12, 20CT27, 20CT51, 20DT09, 20DT37, 20ET16, 20ET56, 20FT10, 20FT54, 20GG36, 20GG45, KME20H0245, KME20H1287, KME20H1288, KME20J0571, KME20J0572, KME20J0802, KME20J3033, KME20K2544, KME20L0053, KME20L0055, KME20L0942, KME20L2372, KME20M0381, KME20M1103, KME20M1755, KME21A0893, KME21B1074, KME21B1075, KME21D1430, KME21E1290, KME21F1526, KME21G0541, KME21G0542, KME21G0543, KME21G1559, KME21H0608, KME21K0551, KME21K1767, KME21K2469, KME21L1897 |

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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## 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-1831-2023%22)

## Related records

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