{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69621",
      "recalling_firm": "Biomerica",
      "address_1": "17571 Von Karman Ave",
      "address_2": "N/A",
      "postal_code": "92614-6207",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- USA, including the states of NH, CA, NJ, FL; and, the countries of Russia, Ukraine, Switzerland, Spain, Italy, Serbia, China, France, Pakistan, Austria, United Kingdom, Egypt, and India.",
      "recall_number": "Z-0467-2015",
      "product_description": "Calcitonin ELISA Kit, Code No. 7024, 7024BU.    Intended use of this product is the quantitative determination of Calcitonin in human serum.",
      "product_quantity": "1,062 units",
      "reason_for_recall": "A potential issue with false high values.",
      "recall_initiation_date": "20140918",
      "center_classification_date": "20141126",
      "termination_date": "20150328",
      "report_date": "20141203",
      "code_info": "Lot No. 2041, 2071, 2089, 2124, 2167, 2178, 2180.",
      "more_code_info": ""
    }
  ]
}