---
title: "Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF ... — FDA record Z-1890-2023 | 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-1890-2023-endotracheal-tube-oral-nasal-murphy-eye-high-volume-low-pressure-cuff-ref-112082080/
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 112082080 — FDA record Z-1890-2023

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 112082080
- **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**: 170179 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1890-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1890-2023%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 14026704341440, Batch Numbers: 18GG11, 18GG12, 18GG13, 18GT08, 18GT11, 18HG40, 18IG04, 18IG07, 18IG12, 18IG13, 18IG23, 18IT06, 18IT10, 18IT16, 18JG07, 18JG09, 18JG13, 18JG26, 18JG37, 18JG38, 18JT06, 18JT10, 19AG35, 19AG38, 19AT20, 19BG06, 19BG07, 19BG14, 19BG18, 19BG22, 19BG25, 19BG30, 19BT08, 19BT12, 19DT36, 19DT43, 19ET22, 19ET27, 19ET82, 19ET83, 19FT04, 19FT13, 19FT26, 19FT28, 19KT14, 19LT46, 19LT47, 19LT51, 20AT22, 20AT49, 20BG15, 20BG19, 20BT05, 20BT09, 20BT10, 20BT24, 20CT42, 20CT48, 20CT54, 20DT10, 20DT23, 20DT28, 20ET16, 20ET17, 20ET39, 20FT17, 20FT43, 20FT49, 20FT58, 20FT61, 20GG48, 20GT10, 20GT11, 20GT12, 20GT23, KME20G0436, KME20H0953, KME20L1706, KME20L2207, KME20L2333, KME20L2607, KME20L2696, KME20M1043, KME20M1342, KME21A1435, KME21A1524, KME21A2058, KME21B0616, KME21D1653, KME21D1946, KME21D2011, KME21D2012, KME21E0584, KME21E0687, KME21E1452, KME21F0981, KME21F1006, KME21F1215, KME21F1530, KME21F1604, KME21G0736, KME21G1100, KME21J0109, KME21J0563, KME21J1295, KME21J1364, KME21J1415, KME21J1532, KME21J2055, KME21K0022, KME21K0187, KME21K0449, KME21K2884, KME21K3013, KME21L0744, KME21L1438, KME21L1533, KME21L1661, KME21L1787, KME21L2012, KME21L2177, KME21M3032, KME21M3137, KME21M3236, KME22A0626, KME22A0793, KME22A1043, KME22A1701, KME22A2203, KME22A2429, KME22A2693, KME22A2966, KME22B0500, KME22B0737, KME22B0898, KME22B0915, KME22B0991, KME22C1987, KME22C2072, KME22C2219, KME22C2400, KME22C3376, KME22D0004, KME22D1589, KME22D1689, KME22D1897, KME22D2014, KME22D2505, KME22D2636, KME22D3062, KME22D3275, KME22D3421, KME22D3427, KME22D3712, KME22E2014, KME22F0621, KME22F2238, KME22J3346, KME22K0540, KME22K0541, KME22K0654, KME22K0691, KME22K0694, KME22K0715, KME22K0777, KME22M0921, KME23A0132, KME23A0714, KME23B1443 |

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-1890-2023%22)

## Related records

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