---
title: "RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040 — FDA record Z-1898-2023 | 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-1898-2023-ruschelit-safety-clear-tracheal-tube-oral-nasal-magill-ref-112480040/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040 — FDA record Z-1898-2023

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**: RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
- **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**: 37076 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1898-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1898-2023%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 14026704341525, Batch Numbers: 18FG14, 18FG22, 18JG08, 18KG25, 18LG04, 18LG30, 19DT35, 19DT36, 19ET09, 19ET31, 19ET51, 19HT60, 19IT32, 19IT43, 20AT06, 20AT39, 20BT01, 20BT53, 20CT12, 20CT27, 20CT54, 20DT04, 20ET30, 20FT58, KME20G0182, KME20H0372, KME20H0373, KME20J0924, KME20J2043, KME21C2368, KME21K1187, KME21K1188, KME21K1977, KME21M1084, KME21M1842, KME21M1845, KME21M2733, KME21M2734, KME21M2735, KME21M2736, KME22B2019, KME22C1693, KME22D0057, KME22D0180, KME22D0819, KME22D1066, KME22D3269, KME22E0602, KME22E2648, KME22E2681, KME22F1440, KME22F1692, KME22F2455, KME22G2312, KME22H1126, KME22H1212, KME22H2302, KME22J1615, KME22K0283, KME22K0632, KME22K1096, KME22M1155, KME22M1478, KME22M1659, KME23B3174 |

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-1898-2023%22)

## Related records

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