---
title: "RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480045 — FDA record Z-1899-2023 | 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-1899-2023-ruschelit-safety-clear-tracheal-tube-oral-nasal-magill-ref-112480045/
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 112480045 — FDA record Z-1899-2023

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 112480045
- **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**: 30391 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1899-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1899-2023%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 14026704341532, Batch Numbers: 18FG02, 18FG14, 18GT16, 18HG37, 18IG13, 18KG34, 18LG03, 19AG04, 19AG08, 19AG23, 19AG38, 19BG35, 19CG05, 19DT09, 19FT12, 19IT38, 19JT19, 19JT21, 19KT58, 19LT09, 19LT27, 20AT06, 20BG15, 20CT07, 20CT12, 20CT54, 20DT01, 20DT09, 20ET30, 20FT58, 20GT22, KME20H0774, KME20J0792, KME20J2687, KME20M0861, KME20M1576, KME20M1925, KME20M1926, KME20M3207, KME21A0769, KME21B0450, KME21C0314, KME21C1807, KME21K1189, KME21K1920, KME21M1895, KME21M2015, KME21M2776, KME21M3038, KME22B2939, KME22C0808, KME22C0928, KME22D0939, KME22D0940, KME22D1836, KME22D2309, KME22F0391, KME22F1537, KME22F2459, KME22F2526, KME22G1183, KME22H0051, KME22H3521, KME22J2886, KME22K1019, KME22M2104, KME23A1068, KME23A1487, KME23A2313 |

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-1899-2023%22)

## Related records

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