---
title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1878-2023 | 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-1878-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781040/
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 111781040 — FDA record Z-1878-2023

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 111781040
- **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**: 347422 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1878-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1878-2023%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 14026704341167, Batch Numbers: 18FT35, 18GG16, 18GG19, 18GG23, 18GG34, 18GT32, 18HG17, 18HG21, 18HG22, 18HG29, 18HG30, 18IG15, 18JG01, 18JG03, 18JG16, 18JG19, 18JG35, 18JG37, 18KG17, 18KG19, 18KG38, 18LG12, 18LG14, 18LG18, 18LG30, 19AG01, 19AG19, 19AG29, 19BG18, 19BG32, 19BG33, 19CG01, 19CG02, 19CT26, 19CT33, 19CT53, 19CT73, 19CT80, 19CT82, 19DT05, 19DT30, 19DT35, 19DT38, 19DT42, 19ET18, 19ET34, 19ET39, 19ET40, 19ET58, 19ET60, 19ET61, 19ET65, 19ET69, 19FT01, 19FT41, 19GT13, 19GT16, 19GT63, 19HT31, 19HT82, 19IT01, 19IT14, 19JT35, 19JT56, 19JT63, 19KT02, 19KT41, 19KT46, 19LT21, 19LT36, 20AT22, 20AT53, 20BT01, 20BT02, 20CT05, 20DT23, 20DT29, 20DT32, 20DT35, 20ET04, 20ET33, 20ET34, 20ET38, 20ET39, 20FT17, 20FT19, 20FT60, 20FT64, 20FT68, 20GT11, 20GT34, KME20H1786, KME20H2999, KME20J0367, KME20J0494, KME20J1209, KME20J1388, KME20M2796, KME20M2906, KME20M2907, KME20M2994, KME20M3092, KME21A1005, KME21A1006, KME21A2030, KME21A2037, KME21A3023, KME21A3024, KME21A3028, KME21A3029, KME21B0259, KME21B0788, KME21B0994, KME21B1198, KME21B1286, KME21B1288, KME21B1620, KME21B2627, KME21B2628, KME21B2705, KME21C0428, KME21C1121, KME21C1199, KME21C1879, KME21C3336, KME21F0980, KME21K1094, KME21K1655, KME21K1714, KME21K1841, KME21K2300, KME21K3006, KME21L2290, KME21L2744, KME21L2745, KME21L2760, KME21L2761, KME21L2787, KME21L2869, KME21M0203, KME21M0801, KME21M0809, KME21M0950, KME21M1706, KME21M1904, KME21M1905, KME21M2908, KME22A0561, KME22A2283, KME22A2404, KME22A2849, KME22A2915, KME22A3199, KME22B0002, KME22B0003, KME22B0004, KME22B0043, KME22B0123, KME22B0124, KME22B0165, KME22B0192, KME22B0545, KME22B0585, KME22B1999, KME22C1877, KME22C1989, KME22C1990, KME22C2189, KME22C2479, KME22C2480, KME22C2481, KME22C2659, KME22C2660, KME22C2760, KME22C2839, KME22C2840, KME22C2866, KME22C2966, KME22C3124, KME22C3126, KME22C3454, KME22D0284, KME22D1566, KME22D1674, KME22D1698, KME22D1813, KME22D1890, KME22D2708, KME22D3011, KME22E0730, KME22E0731, KME22E0945, KME22E1105, KME22E1394, KME22E1499, KME22E1933, KME22E2376, KME22E2659, KME22E2810, KME22E2889, KME22F0001, KME22F0541, KME22F2997, KME22F3120, KME22F3243, KME22F3423, KME22G0815, KME22G1098, KME22G1167, KME22G1228, KME22G1229, KME22G1330, KME22G2240, KME22G2307, KME22G2576, KME22G2629, KME22G2924, KME22G3134, KME22H0545, KME22H0600, KME22H0761, KME22H1361, KME22H1725, KME22H1932, KME22H2056, KME22H2520, KME22H3068 |

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-1878-2023%22)

## Related records

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