---
title: "Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535 — FDA record Z-1856-2023 | 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-1856-2023-flexi-set-uncuffed-endotracheal-tube-and-stylet-set-oral-nasal-ref-506535/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535 — FDA record Z-1856-2023

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**: Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535
- **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**: 18353 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1856-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1856-2023%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 4026704547685, Batch Numbers: 18FG05, 18FG20, 18GG12, 18GG17, 18GG28, 18GT32, 18HG12, 18HG16, 18JG17, 18KG07, 18LG02, 18LG22, 18LG28, 19AG21, 19BG40, 19CT58, 19ET38, 19ET60, 19ET72, 19FT01, 19GT05, 19GT10, 19GT20, 19GT45, 19GT59, 19GT65, 19HT05, 19HT40, 19HT61, 19HT80, 19IT29, 19JT49, 19KT08, 19LT04, 19LT48, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT22, 20CT36, 20CT44, 20DT14, 20DT37, 20ET16, 20ET21, 20ET28, 20FT44, KME20K1624, KME20K3589, KME20L0616, KME20L0617, KME20M2049, KME20M3274, KME20M3275, KME20M3278, KME21A1899, KME21A2809, KME21B0575, KME21C0027, KME21C0491, KME22A0057, KME22A0206, KME22B0539, KME22B0725, KME22B1028, KME22B1562, KME22C0916, KME22C1821, KME22C1940, KME22D0350, KME22D1078, KME22F0162, KME22F2162, KME22G3101, KME22G3233, KME22H2624, KME22J0803, KME22J3077 |

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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- [Utah](https://isitonrecall.com/state/utah/)
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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-1856-2023%22)

## Related records

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