---
title: "Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF ... — FDA record Z-1887-2023 | 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-1887-2023-endotracheal-tube-oral-nasal-murphy-eye-high-volume-low-pressure-cuff-ref-112082065/
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 112082065 — FDA record Z-1887-2023

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 112082065
- **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**: 247645 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1887-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1887-2023%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 14026704341419, Batch Numbers: 18FG23, 18FG27, 18FG30, 18FG31, 18FT06, 18FT08, 18GG19, 18GT32, 18GT34, 18HG02, 18HG15, 18IG02, 18IG07, 18IG13, 18IT25, 18JG01, 18JG02, 18JG04, 18JG07, 18JG20, 18KG44, 18KT28, 18LG14, 19AG09, 19AG15, 19AG32, 19AG33, 19AT20, 19BG14, 19BG18, 19BG40, 19CG07, 19CT26, 19CT39, 19CT40, 19CT76, 19DT10, 19DT16, 19DT27, 19DT47, 19ET02, 19ET05, 19ET65, 19GT19, 19GT29, 19GT30, 19GT31, 19GT38, 19HT26, 19HT61, 19HT66, 19HT68, 19IT20, 19IT33, 19IT59, 19JT18, 19JT19, 19JT26, 19JT32, 19JT36, 19JT49, 19JT63, 19KT20, 19KT21, 19KT26, 19LT07, 19LT31, 19LT46, 20AT05, 20AT06, 20AT20, 20AT47, 20AT49, 20BT13, 20CT02, 20CT13, 20CT23, 20CT37, 20CT47, 20CT54, 20DT01, 20DT02, 20ET16, 20ET18, 20GT05, 20GT06, 20GT13, 20GT22, 20GT24, KME20H0882, KME20H2726, KME20H2934, KME20J1386, KME20J1399, KME20J1656, KME20K0036, KME20K0259, KME20K0436, KME20K0504, KME20K0677, KME20K0881, KME20L2349, KME20L2447, KME20L2448, KME20M0710, KME20M0892, KME20M0928, KME20M1806, KME20M1923, KME20M2249, KME20M2450, KME20M2708, KME21A0338, KME21A0404, KME21A0695, KME21B1352, KME21B2607, KME21B2789, KME21C0504, KME21C0981, KME21C0983, KME21C1035, KME21C1097, KME21E0607, KME21E0685, KME21F0384, KME21F0516, KME21F0694, KME21F0834, KME21F0930, KME21F1554, KME21F1885, KME21F2156, KME21F2203, KME21G0532, KME21H0202, KME21H0916, KME21H1233, KME21H1264, KME21J0302, KME21J0389, KME21J0528, KME21J0637, KME21J0725, KME21J0909, KME21J1871, KME21J1945, KME21J1998, KME21K0570, KME21K0587, KME21K0829, KME21L0344, KME21L0408, KME21L0566, KME21L1306, KME21L2132, KME21L2653, KME21M0853, KME21M1380, KME21M1469, KME22A0676, KME22A1234, KME22A1388, KME22A1505, KME22A2005, KME22A2059, KME22A2198, KME22A2316, KME22A2350, KME22A2401, KME22A2481, KME22A2694, KME22A2959, KME22A3224, KME22B0070, KME22B0466, KME22B0566, KME22B0946, KME22B1049, KME22B1945, KME22B2102, KME22B2322, KME22B2644, KME22C2076, KME22D0407, KME22D0573, KME22D0810, KME22D1482, KME22D1780, KME22D2011, KME22D2630, KME22D3020, KME22E1854, KME22E2488, KME22F1264, KME22F2116, KME22F2172, KME22F2296, KME22F2720, KME22G0552, KME22G2426, KME22G2943, KME22H0766, KME22H1917, KME22H2054 |

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-1887-2023%22)

## Related records

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