{
  "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,
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    }
  },
  "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-3001-2018",
      "product_description": "iView DAB Detection Kit w/o Secondary Antibody, Catalog Number 05266173001, Model 760-093.     For laboratory use.",
      "product_quantity": "10 units",
      "reason_for_recall": "Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers.  A false negative IHC result may occur.",
      "recall_initiation_date": "20180802",
      "center_classification_date": "20180914",
      "termination_date": "20211122",
      "report_date": "20180926",
      "code_info": "Lot Number:  Y19981,  UDI: 4015630970261"
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}