Kamiya Biomedical Company K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013 recall — FDA Z-0271-2023
IgA Reagent may start showing cloudiness over time, which can affect assay performance.
Overview of recall records associated with Kamiya Biomedical Company, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
IgA Reagent may start showing cloudiness over time, which can affect assay performance.
This page summarizes recall records in which the official source identifies Kamiya Biomedical Company, LLC 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.