# FDA recall Z-1703-2025

> **IBA Dosimetry GmbH** · Class II · device recall initiated 2025-04-01.

## Product

myQA iON; Article Number: MQ10-000;

## Reason for recall

Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.

## 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.

## Key facts

- **Recall number:** Z-1703-2025
- **Recalling firm:** IBA Dosimetry GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-01
- **Report date:** 2025-05-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Schwarzenbruck, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1703-2025

## Citation

> AI Analytics. FDA recall Z-1703-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1703-2025. Source: US FDA. Licensed CC0.

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