FDA Device recall Z-1703-2025
myQA iON
- FDA Device
- Class II
- ongoing
- Published 2025-05-07
On 2025-05-07 the FDA classified a Class II recall of myQA iON by Iba Dosimetry, citing wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1703-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-04-01 |
| Published | 2025-05-07 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Iba Dosimetry |
| Distribution | US |
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.
Identifiers
| code_info | Article Number: MQ10-000; UDI-DI: EIBAMQ010000; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1703-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.