---
title: "Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030 — FDA record Z-1874-2023 | 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-1874-2023-endotracheal-tube-oral-nasal-uncuffed-plain-murphy-ref-100382030/
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 100382030 — FDA record Z-1874-2023

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 100382030
- **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**: 25160 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1874-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1874-2023%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 14026704340795, Batch Numbers: 18FT13, 18GT32, 18HG08, 18HG25, 18IG29, 18JG35, 18KG08, 18LG23, 19AG08, 19AG23, 19AG38, 19BG12, 19BG35, 19CT37, 19CT42, 19DT36, 19ET51, 19FT08, 19GT05, 19GT35, 19IT11, 19IT56, 19KT13, 19LT27, 20AT05, 20BT43, 20CT07, 20DT22, 20ET30, 20FT43, 20FT55, 20GT18, KME20K0276, KME20M3220, KME21A0764, KME21C0890, KME21C1020, KME21C1033, KME21C1572, KME21C2686, KME21D1293, KME21D1448, KME21D1743, KME21D1913, KME21F0962, KME22A2454, KME22C1763, KME22D2425, KME22D2823, KME22E0291, KME22E0560, KME22E2506, KME22E2684, KME22E2925, KME22F1606, KME22J1478, KME22K0878, KME22L2920, KME22M0084, KME22M0213 |

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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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [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-1874-2023%22)

## Related records

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