{
  "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": "Lenexa",
      "state": "KS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78470",
      "recalling_firm": "Remel Inc",
      "address_1": "12076 Santa Fe Trail Dr",
      "address_2": "N/A",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to AL, MD, ME, NC, and TN.  There was no foreign/military/government distribution.",
      "recall_number": "Z-0209-2018",
      "product_description": "CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.",
      "product_quantity": "7 units",
      "reason_for_recall": "Product may have incorrect cation information detailed on the product label.",
      "recall_initiation_date": "20171102",
      "center_classification_date": "20171207",
      "termination_date": "20200805",
      "report_date": "20171213",
      "code_info": "Lot 1865331, Exp. 06/2021",
      "more_code_info": ""
    }
  ]
}