{
  "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": "Blue Earth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70008",
      "recalling_firm": "Express Diagnostics Int'l., Inc.",
      "address_1": "1550 Industrial Dr",
      "address_2": "N/A",
      "postal_code": "56013-1100",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- US, including the states of CA, NY, MN, and SC; SWEDEN, CANADA, UNITED KINGDOM, and GUATEMALA.",
      "recall_number": "Z-1033-2015",
      "product_description": "DrugCheck Ketamine Dip Test  31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT.      This assay provides only a preliminary analytical test result.",
      "product_quantity": "5,050",
      "reason_for_recall": "This recall has been initiated due to potential false positives results when using the test to screen for Ketamine. Use of this product may give incorrect screening results.",
      "recall_initiation_date": "20141121",
      "center_classification_date": "20150130",
      "termination_date": "20190514",
      "report_date": "20150211",
      "code_info": "PC 09077, PC03227, PC03055, PC09293, PC11115, PC08126, PC06276, PC07085, PC06305, and PC08017."
    }
  ]
}