myQA iON recall
myQA iON; Article Number: MQ10-000;
Why was myQA iON recalled?
Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Article Number: MQ10-000; UDI-DI: EIBAMQ010000;
- Product
- myQA iON; Article Number: MQ10-000;
- Recalling firm
- IBA Dosimetry GmbH
- 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, Philippines, South Korea, Thailand.
- Recall date
- May 7, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)