{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tukwila",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91030",
      "recalling_firm": "Kamiya Biomedical Company, LLC",
      "address_1": "12779 Gateway Dr S",
      "address_2": "N/A",
      "postal_code": "98168-3308",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of FL, NC, TX, TN, PA, CA, NY, IL, MA and the country of Czech Republic.",
      "recall_number": "Z-0271-2023",
      "product_description": "K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013",
      "product_quantity": "165",
      "reason_for_recall": "IgA Reagent may start showing cloudiness over time, which can affect assay performance.",
      "recall_initiation_date": "20220928",
      "center_classification_date": "20221121",
      "report_date": "20221130",
      "code_info": "UDI-DI: 00816426020092, Lot/ Expiration Date: H180/ 2023-01-31, K181/ 2023-03-31, N182/ 2023-06-30, D283/ 2023-09-30"
    }
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}