{
  "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": "Santa Clara",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67665",
      "recalling_firm": "LumiQuick Diagnostics Inc.",
      "address_1": "2946 Scott Blvd",
      "address_2": "N/A",
      "postal_code": "95054-3312",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of CA, FL, NJ, TX, and NY.",
      "recall_number": "Z-1412-2014",
      "product_description": "Cardiac Panel Test Card (Whole Blood);    LumiQuick,.  Santa Clara, CA  95054",
      "product_quantity": "ALL",
      "reason_for_recall": "Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.",
      "recall_initiation_date": "20140304",
      "center_classification_date": "20140407",
      "termination_date": "20140509",
      "report_date": "20140416",
      "code_info": "Catalog number: 75004, All lots"
    }
  ]
}