---
title: "RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035 — FDA record Z-1897-2023 | 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-1897-2023-ruschelit-safety-clear-tracheal-tube-oral-nasal-magill-ref-112480035/
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 112480035 — FDA record Z-1897-2023

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 112480035
- **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**: 31945 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1897-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1897-2023%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 14026704341518, Batch Numbers: 18GG15, 18GG16, 18IG01, 18IG03, 18IG04, 18IG13, 18LG30, 19BG16, 19BG35, 19DT35, 19ET51, 19GT51, 19IT38, 19JT20, 19JT50, 19KT37, 19KT60, 19LT03, 19LT27, 20AT54, 20BT42, 20BT51, 20CT07, 20CT54, 20ET30, 20FT43, KME20H2894, KME20J0754, KME20J3097, KME20M2591, KME20M3049, KME20M3050, KME21A0349, KME21A3147, KME21A3239, KME21B1099, KME21C1766, KME21C2690, KME21C3242, KME21D0295, KME21D2960, KME21K1922, KME21M0820, KME21M2050, KME21M3073, KME22A0416, KME22A1499, KME22B2850, KME22C1453, KME22C1455, KME22C2694, KME22D1761, KME22D2536, KME22E0601, KME22F2453, KME22G0614, KME22G1180, KME22G1181, KME22G1876, KME22H2913, KME22H3442, KME22J2322, KME22J3348, KME22L1190, KME22L1191, KME22L1547, KME23A2353, KME23A2534, KME23B0590, KME23C0083 |

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-1897-2023%22)

## Related records

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