{
  "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": "Oro Valley",
      "state": "AZ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80807",
      "recalling_firm": "Ventana Medical Systems Inc",
      "address_1": "1910 E Innovation Park Dr",
      "address_2": "N/A",
      "postal_code": "85755-1962",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "worldwide",
      "recall_number": "Z-3008-2018",
      "product_description": "VENTANA ISH iView Blue Detection Kit, Catalog Number 05278511001, model 800-092     Immunohistochemistry (IHC) for in vitro diagnostic use.",
      "product_quantity": "559 units",
      "reason_for_recall": "Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers",
      "recall_initiation_date": "20180802",
      "center_classification_date": "20180914",
      "termination_date": "20211122",
      "report_date": "20180926",
      "code_info": "Lot Numbers:  Y15105, Y22455, UDI: 4015630971930"
    }
  ]
}