IBA Dosimetry GmbH 2025-05-07 Health serious FDA
Health · FDA · Recall #FDA-Z-1703-2025
myQA iON; Article Number: MQ10-000; Recall
Issued May 7, 2025 · IBA Dosimetry GmbH
In May 2025, IBA Dosimetry GmbH recalled the myQA iON; Article Number: MQ10-000;, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
What you should do
- 1 Stop using myQA iON; Article Number: MQ10-000; right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact IBA Dosimetry GmbH to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- IBA Dosimetry GmbH
- Category
- Health
- Recall date
- May 7, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution in the states of AL, AR, FL, GA, KS, MD, OK and the countries of Algeria, Austria, Belgium, Czech Rep
- Recall number
- FDA-Z-1703-2025
- Made in
- Germany
- Issuing agency
- FDA
In context
- IBA Dosimetry GmbH has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.