---
title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1953-2023 | 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-1953-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781055/
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 111781055 — FDA record Z-1953-2023

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 111781055
- **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**: 172721 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1953-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1953-2023%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 14026704341198, Batch Numbers: 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, 18IG10, 18IG16, 18IG17, 18JG13, 18JG20, 18JG35, 18JG37, 18KG18, 18KG39, 18KG41, 18LG12, 18LG14, 18LG30, 18LG39, 19AG29, 19BG03, 19BG04, 19BG18, 19BG19, 19BG33, 19CG01, 19CG02, 19CG04, 19CT28, 19CT33, 19CT56, 19DT03, 19DT30, 19DT35, 19DT42, 19DT46, 19ET16, 19ET34, 19FT01, 19GT63, 19HT31, 19HT55, 19IT01, 19IT12, 19IT14, 19IT15, 19IT19, 19KT02, 19KT41, 19LT17, 20BT01, 20BT02, 20CT07, 20DT18, 20DT29, 20DT32, 20ET34, 20ET49, 20FT18, 20FT64, 20GT11, 20GT34, 20GT49, KME20H0487, KME20H1788, KME20H2574, KME20H2768, KME20H3002, KME20J1213, KME20L0905, KME20L2170, KME20L2191, KME20L2670, KME20M0304, KME20M2647, KME20M3094, KME21A1082, KME21A2080, KME21A2926, KME21B0543, KME21B1199, KME21B1630, KME21B1716, KME21B2541, KME21B2670, KME21C0592, KME21C0593, KME21C3340, KME21D2002, KME21E0008, KME21E0009, KME21F0901, KME21F1424, KME21F1459, KME21F2371, KME21J1239, KME21J1487, KME21J1691, KME21J1692, KME21J1854, KME21K0178, KME21K1046, KME21K1078, KME21K2304, KME21K3005, KME21L0631, KME21L0756, KME21L1428, KME21L1429, KME21L1596, KME21L2141, KME21L2291, KME21L2736, KME22A1889, KME22A1890, KME22A2018, KME22A2281, KME22A2921, KME22A2969, KME22B0359, KME22C0207, KME22C2843, KME22C2927, KME22C2969, KME22C3213, KME22C3304, KME22C3375, KME22C3379, KME22D0052, KME22D0587, KME22D0719, KME22D0808, KME22D0844, KME22D0846, KME22D0855, KME22D0899, KME22D1001, KME22D1093, KME22D1115, KME22D1337, KME22D1348, KME22D1454, KME22D1568, KME22D1675, KME22D1820, KME22D2489, KME22D2490, KME22D3014, KME22D3071, KME22E1106, KME22E1398, KME22E1402, KME22E1502, KME22E1580, KME22E1581, KME22E1629, KME22E1778, KME22E1851, KME22E1931, KME22E2306, KME22F0073, KME22F0543, KME22F1077, KME22G1333, KME22G2578, KME22H1508, KME22H2499, KME22H3402, KME22K0250 |

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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- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
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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-1953-2023%22)

## Related records

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