---
title: "Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035 — FDA record Z-1875-2023 | 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-1875-2023-endotracheal-tube-oral-nasal-uncuffed-plain-murphy-ref-100382035/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035 — FDA record Z-1875-2023

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 uncuffed/plain - Murphy, REF 100382035
- **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**: 25435 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1875-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1875-2023%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 14026704340801, Batch Numbers: 18GG15, 18GT32, 18IG13, 18KG24, 18KG33, 18KG34, 18LG01, 18LG03, 19CG05, 19CT36, 19CT72, 19DT13, 19KT20, 20AT05, 20AT50, 20BG19, 20BT43, 20DT01, 20DT04, 20DT24, 20ET30, 20FT21, 20FT43, 20FT58, 20FT68, 20GT22, KME20G0092, KME20K0870, KME20L1581, KME20L1894, KME20M3043, KME21B0039, KME21B1553, KME21C0891, KME21C0930, KME21C1580, KME21L2524, KME22B0933, KME22C2632, KME22C2804, KME22D1106, KME22D2022, KME22D2157, KME22D2462, KME22D2650, KME22D3220, KME22D3334, KME22E0292, KME22E0669, KME22E2685, KME22E2686, KME22F1707, KME22F2556, KME22H1215, KME22J2124, KME22K0712, KME22K0713, KME22K1577, KME22K2171, KME22K2382, KME22K2545, KME22L1846, KME22L2147, KME22L2341, KME22L2372, KME22L2411, KME22M1269, KME22M2426 |

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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- [Utah](https://isitonrecall.com/state/utah/)
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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-1875-2023%22)

## Related records

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