IBA Dosimetry GmbH myQA iON; Article Number: MQ10-000 recall — FDA Z-1703-2025
Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
Overview of recall records associated with IBA Dosimetry GmbH, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
This page summarizes recall records in which the official source identifies IBA Dosimetry GmbH as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.