Class II — IBA Dosimetry GmbH
| Recalling firm | IBA Dosimetry GmbH |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character. |
| Product | myQA iON; Article Number: MQ10-000; |
| Quantity | 84 units (9US, 75 OUS) |
| 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, Phili… |
| Initiated | 2025-04-01 |
| Classified | 2025-04-30 |
| Recall number | Z-1703-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — IBA Dosimetry GmbH (Z-1703-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96647/
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