---
title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1955-2023 | 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-1955-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781065/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065 — FDA record Z-1955-2023

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**: Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065
- **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**: 37890 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1955-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1955-2023%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 14026704341211, Batch Numbers: 18FG20, 18FG31, 18GG17, 18HG21, 18IG16, 18IG30, 18JG16, 18JG20, 18KG01, 18LG30, 19AG01, 19AG25, 19AG29, 19BG18, 19CG02, 19DT35, 19DT46, 19ET36, 19FT01, 19FT02, 19FT45, 19GT63, 19HT55, 19HT68, 19IT53, 19KT14, 19KT46, 19LT17, 19LT21, 20AT22, 20BT01, 20CT11, 20CT32, 20DT19, 20ET39, 20FT18, 20FT64, KME20H0432, KME20H2681, KME20L2673, KME20M1288, KME20M2831, KME20M2957, KME21A2081, KME21A2935, KME21B0719, KME21B1201, KME21B1825, KME21B1947, KME21C0646, KME21C1045, KME21C3350, KME21D1229, KME21E0011, KME21F0146, KME21K1657, KME21K1658, KME21K1713, KME21K1748, KME21L2302, KME21L2792, KME21L2886, KME22A1379, KME22A1884, KME22A1885, KME22A2922, KME22C0332, KME22C0413, KME22C1125, KME22C1127, KME22C1581, KME22C2971, KME22D0261, KME22D1843, KME22D3133, KME22E0948, KME22E0949, KME22F0366, KME22F0988, KME22F3121, KME22G0692, KME22G1335, KME22G3063, KME22H0521, KME22H1633, KME22H3274, KME22J0144, KME22J1123, KME22J2413, KME22J2479, KME22K0090 |

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-1955-2023%22)

## Related records

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