---
title: "AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a batter... — FDA record Z-0279-2025 | Is It on Recall"
description: "Values used to calibrate whole blood oximeter instruments were observed to be higher than normal, which may result in incorrect patient results where oxygen lev"
url: https://isitonrecall.com/recall/fda-device-z-0279-2025-avoximeter-1000e-product-number-avox1000e-the-avoximeter-1000e-is-a-battery-operated-bedside-whole-b/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter. — FDA record Z-0279-2025

Reported completed

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 27, 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**: AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter.
- **Reason**: Values used to calibrate whole blood oximeter instruments were observed to be higher than normal, which may result in incorrect patient results where oxygen levels are higher than actual results, which may lead to patient care mismanagement requiring medical intervention.
- **Classification**: Class II
- **Recalling firm**: Accriva Diagnostics, Inc.
- **Quantity**: 1
- **Agency-reported status**: Completed
- **Source record identifier**: Z-0279-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0279-2025%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: 10711234530023. Serial Number: 6824 |

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

## Distribution

US: AZ

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

- [Arizona](https://isitonrecall.com/state/arizona/)

## Dates in the source

- **Report date**: Nov 6, 2024
- **Recall initiation date**: Sep 27, 2024
- **Center classification date**: Oct 31, 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-0279-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Accriva Diagnostics, Inc. records](https://isitonrecall.com/brand/accriva-diagnostics-inc/)