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Kamiya Biomedical Company, LLC recalls K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
Recalled November 30, 2022 · FDA recall Z-0271-2023 · Kamiya Biomedical
Hazard
IgA Reagent may start showing cloudiness over time, which can affect assay performance. · FDA Class II
Units
165
Sold at
Worldwide - US Nationwide distribution in the states of FL, NC, TX, TN, PA, CA, NY, IL, MA and the country of Czech Republic.
Description
IgA Reagent may start showing cloudiness over time, which can affect assay performance.
Product
K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
Manufacturer(s)
Kamiya Biomedical Company, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →