---
title: "myQA iON; Article Number: MQ10-000; — FDA record Z-1703-2025 | Is It on Recall"
description: "Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character."
url: https://isitonrecall.com/recall/fda-device-z-1703-2025-myqa-ion-article-number-mq10-000/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# myQA iON; Article Number: MQ10-000; — FDA record Z-1703-2025

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 1, 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**: myQA iON; Article Number: MQ10-000;
- **Reason**: Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
- **Classification**: Class II
- **Recalling firm**: IBA Dosimetry GmbH
- **Quantity**: 84 units (9US, 75 OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1703-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1703-2025%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 | Article Number: MQ10-000; UDI-DI: EIBAMQ010000; |

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

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, FL, GA, KS, MD, OK and the countries of Algeria, Austria, Belgium, Czech Republic, Denmark, France, Germany, Ireland, Italy, Morocco, Norway, Poland, Slovakia, Spain, Israel, Kazakhstan, Kosovo, Libya, South Africa, Turkey, United Kingdom, Switzerland, Argentina, Brazil, Mexico, APAC: Indonesia, Japan, Peoples Republic of China, Philippines, South Korea, Thailand.

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**: May 7, 2025
- **Recall initiation date**: Apr 1, 2025
- **Center classification date**: Apr 30, 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-1703-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [IBA Dosimetry GmbH records](https://isitonrecall.com/brand/iba-dosimetry-gmbh/)
