---
title: "NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I — FDA record Z-0029-2026 | Is It on Recall"
description: "The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for"
url: https://isitonrecall.com/recall/fda-device-z-0029-2026-noxboxi-nitric-oxide-delivery-system-model-numbers-noxbox-i/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I — FDA record Z-0029-2026

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 Sep 9, 2025. 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**: NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
- **Reason**: The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to user prompts.
- **Classification**: Class I
- **Recalling firm**: NOXBOX LTD
- **Quantity**: 1667 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0029-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0029-2026%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 | Model Numbers: (1) NOXBOXI (NBL (Manufacturer)), (2) REQNOXBOXI (Linde (U.S. Distributor)); UDI-DI: 05060541640009; All serial numbers. |

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

## Distribution

Domestic: TN;

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

- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Oct 15, 2025
- **Recall initiation date**: Sep 9, 2025
- **Center classification date**: Oct 6, 2025

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-0029-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [NOXBOX LTD records](https://isitonrecall.com/brand/noxbox-ltd/)