---
title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1954-2023 | 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-1954-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781060/
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 111781060 — FDA record Z-1954-2023

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 111781060
- **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**: 43571 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1954-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1954-2023%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 14026704341204, Batch Numbers: 18FT39, 18GT32, 18HG19, 18IG10, 18IG16, 18IG30, 18JG35, 18LG15, 18LG30, 19AG15, 19AG25, 19CT33, 19CT36, 19DT35, 19DT46, 19ET34, 19ET69, 19FT01, 19GT13, 19GT17, 19GT63, 19HT68, 19IT01, 19IT53, 19JT15, 19JT35, 19KT41, 19LT21, 19LT36, 20AT22, 20BT02, 20CT32, 20DT35, 20ET34, 20ET39, 20FT18, 20FT64, KME20H0431, KME20L2192, KME20M0306, KME20M1285, KME20M2828, KME20M2905, KME21A1085, KME21A2932, KME21A3056, KME21B0722, KME21B1047, KME21B1628, KME21B2706, KME21C1054, KME21C2465, KME21C3344, KME21D2006, KME21D2007, KME21F1423, KME21J1549, KME21K3004, KME21L1432, KME21L2739, KME21M0028, KME21M0163, KME21M0799, KME21M2429, KME21M2911, KME21M3080, KME22A0809, KME22A1219, KME22B1419, KME22C1123, KME22C1555, KME22C1556, KME22C2192, KME22C2845, KME22C2970, KME22D0540, KME22D1570, KME22D1620, KME22D1841, KME22D2294, KME22D2491, KME22E2435, KME22E2436, KME22E2874, KME22G0208, KME22G0690, KME22G0862, KME22G1268, KME22G2247, KME22G2660, KME22G3252, KME22H1630, KME22H2409, KME22J1083, KME22J2876 |

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-1954-2023%22)

## Related records

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