Drug recall
myQA iON; Article Number: MQ10-000;
FDA recall event 96647 · Class II · IBA Dosimetry GmbH
Key facts
| Event ID | 96647 |
|---|---|
| Recall numbers | Z-1703-2025 |
| Recalling firm | IBA Dosimetry GmbH |
| Product type | Devices |
| Products | myQA iON; Article Number: MQ10-000; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Apr 1, 2025 |
| Report date | May 7, 2025 |
| City | Schwarzenbruck |
| Country | Germany |
| FEI number | 3006653576 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: