{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80441",
      "recalling_firm": "Diamedix Corporation",
      "address_1": "14100 Nw 57th Ct",
      "address_2": "N/A",
      "postal_code": "33014-3107",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AZ, CA, FL, IL, IN, KY, MA, MI, MN, MO, NH, NJ, NY, OH, OK, PA, RI, TN, TX, and WI",
      "recall_number": "Z-2574-2018",
      "product_description": "Diamedix Is-EBV-EA-D IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-640",
      "product_quantity": "147",
      "reason_for_recall": "Contains a gel-like contaminant that may affect product performance.",
      "recall_initiation_date": "20180105",
      "center_classification_date": "20180728",
      "termination_date": "20191105",
      "report_date": "20180808",
      "code_info": "Lot T0006 Exp. 05/31/2018"
    }
  ]
}