---
title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1951-2023 | 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-1951-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781035/
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 111781035 — FDA record Z-1951-2023

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 111781035
- **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**: 76060 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1951-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1951-2023%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/I 14026704341150, Batch Numbers: 18FG20, 18FG31, 18GG23, 18GG34, 18GT32, 18HG17, 18IG15, 18JG01, 18JG16, 18JG35, 18KG17, 18KG18, 18KG36, 18LG15, 18LG30, 18LG39, 19AG15, 19BG33, 19CG01, 19CG02, 19CT26, 19DT03, 19DT30, 19DT38, 19ET58, 19ET69, 19FT37, 19FT46, 19IT53, 19JT10, 19KT14, 19KT46, 19LT16, 20AT22, 20AT26, 20CT11, 20CT32, 20DT19, 20DT32, 20ET34, 20ET49, 20FT18, 20FT64, 20GT11, KME20H0466, KME20H2769, KME20H2998, KME20H3129, KME20M0650, KME20M1283, KME20M2799, KME20M2822, KME21A2028, KME21A3020, KME21B1044, KME21B1197, KME21B1960, KME21B1961, KME21C0324, KME21C0426, KME21C1119, KME21L0024, KME21L0026, KME21L1782, KME21L2301, KME21L2785, KME21M1710, KME21M2600, KME21M2601, KME22A0560, KME22A0755, KME22A1376, KME22C0493, KME22D1697, KME22D2626, KME22D2999, KME22D3173, KME22D3253, KME22E0727, KME22E0728, KME22E1011, KME22E1155, KME22E1392, KME22E2151, KME22E2239, KME22E2744, KME22E2753, KME22F0075, KME22F0229, KME22F0540, KME22F0600, KME22F0880, KME22F1315, KME22F1736, KME22F2068, KME22F2353, KME22F2627, KME22F2949, KME22F3119, KME22F3242, KME22F3425, KME22G0214, KME22G0600, KME22G0898, KME22G1642, KME22G1861, KME22G2270, KME22G3150, KME22G3268, KME22H2027, KME22H3065, KME22H3272, KME22H3273, KME22H3400, KME22J0633, KME22J0901 |

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-1951-2023%22)

## Related records

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