---
title: "Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF ... — FDA record Z-1884-2023 | 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-1884-2023-endotracheal-tube-oral-nasal-murphy-eye-high-volume-low-pressure-cuff-ref-112082050/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050 — FDA record Z-1884-2023

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**: Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
- **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**: 47520 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1884-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1884-2023%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 14026704341389, Batch Numbers: 18GG02, 18GG19, 18GG23, 18GT06, 18JG04, 18JG15, 18JG16, 18JG18, 18JT06, 18JT16, 19AG33, 19AT20, 19BG02, 19BG03, 19BG10, 19BG15, 19BG22, 19BG26, 19BG42, 19BT04, 19CT25, 19CT82, 19DT05, 19FT38, 19IT26, 19JT18, 19LT13, 19LT17, 19LT50, 20AT13, 20AT40, 20BT38, 20CT02, 20CT12, 20CT43, 20DT13, 20ET12, 20ET17, 20ET56, 20FT23, 20GG47, 20GT32, KME20J1385, KME21G1704, KME21G1949, KME21K0151, KME21K0292, KME21M2075, KME21M2306, KME21M2649, KME22A1589, KME22A2197, KME22B1848, KME22B2478, KME22B2538, KME22B2578, KME22B2692, KME22C0066, KME22C0571, KME22D0281, KME22D2503, KME22D2504, KME22E0316, KME22E1277, KME22E1422, KME22E2743, KME22E2879, KME22G0063, KME22J0616, KME22J1331, KME22J1463, KME22K0660, KME22L1657, KME23A2133, KME23A2214, KME23A2221, KME23A2299, KME23A2358, KME23C0172 |

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-1884-2023%22)

## Related records

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