---
title: "Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-7073... — FDA record Z-1730-2024 | Is It on Recall"
description: "Potential of the nozzle separating during patient use."
url: https://isitonrecall.com/recall/fda-device-z-1730-2024-vyaire-medical-gmbh-vyaire-twin-tube-sample-line-240-cm-model-number-v-707327-the-twintube-sample-li/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327; The TwinTube sample line 240cm is us... — FDA record Z-1730-2024

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 Apr 8, 2024. 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**: Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327; The TwinTube sample line 240cm is used in the Vyntus CPX. The TwinTube sample line 240cm is connected to the adapter for DVT. Twin Tube Probenschlauch (707004), which is sold outside the US only. Used in breath analysis for metabolic response study.
- **Reason**: Potential of the nozzle separating during patient use.
- **Classification**: Class I
- **Recalling firm**: Vyaire Medical, Inc.
- **Quantity**: 649 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1730-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1730-2024%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 14250892903603, All lots prior to June 2023 or with a serial number before 04I00122 are potentially affected. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US nationwide distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Hawaii](https://isitonrecall.com/state/hawaii/)
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- [Kansas](https://isitonrecall.com/state/kansas/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
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- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: May 15, 2024
- **Recall initiation date**: Apr 8, 2024
- **Center classification date**: May 8, 2024

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-1730-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Vyaire Medical, Inc. records](https://isitonrecall.com/brand/vyaire-medical-inc/)
