---
title: "Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530 — FDA record Z-1855-2023 | 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-1855-2023-flexi-set-uncuffed-endotracheal-tube-and-stylet-set-oral-nasal-ref-506530/
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 506530 — FDA record Z-1855-2023

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 506530
- **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**: 32553 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1855-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1855-2023%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 4026704547678, Batch Numbers: 18FG05, 18GG12, 18GG17, 18GG31, 18GT32, 18HG12, 18HG16, 18IG02, 18IG06, 18IG15, 18IG21, 18IG27, 18JG02, 18JG23, 18JG32, 18JG34, 18KG15, 18KG23, 18LG02, 18LG22, 18LG28, 19AG21, 19AG24, 19AG27, 19AG37, 19BG25, 19BG40, 19CT65, 19ET72, 19FT01, 19GT05, 19GT20, 19GT59, 19GT65, 19HT40, 19HT61, 19HT80, 19IT29, 19IT39, 19JT18, 19JT22, 19JT29, 19JT49, 19JT57, 19KT08, 19LT04, 19LT48, 20AT09, 20AT32, 20AT44, 20AT46, 20AT53, 20BT23, 20BT37, 20BT47, 20CT05, 20CT12, 20CT36, 20DT37, 20ET16, 20ET28, KME20J0318, KME20K0152, KME20K0153, KME20K0154, KME20K3587, KME20L1467, KME20L1468, KME20L1838, KME20M2048, KME20M2480, KME21A0669, KME21A1897, KME21A2807, KME21B1674, KME21B1675, KME21C0489, KME21M0865, KME21M2740, KME21M2741, KME22B2144, KME22B2326, KME22B2327, KME22C1075, KME22C1826, KME22C3192, KME22D0787, KME22E0223, KME22E1029, KME22F0563, KME22G0910, KME22G0911, KME22H0780, KME22H2909, KME22J0577, KME22K0015, KME22K0016, KME22K0202, KME22K0335, KME22K0918 |

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.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [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-1855-2023%22)

## Related records

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