{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Earth City",
      "address_1": "13600 Shoreline Dr",
      "reason_for_recall": "Failed Dissolution Specification; at the 6-month stability time point",
      "address_2": "",
      "product_quantity": "94,584 cartons",
      "code_info": "Lot A369286, exp. date 31 Jan 2016",
      "center_classification_date": "20141017",
      "distribution_pattern": "Nationwide including Puerto Rico.",
      "state": "MO",
      "product_description": "Bystolic (nebivolol) tablets, 20 mg/tablet, packaged as 7 tablets/bottle/carton, and 12 bottles/trays, Professional Sample, Rx only, Forest Pharmaceuticals, Inc., St. Louis, MO. ---  NDC 0456-1420-07",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Forest Pharmaceuticals Inc",
      "recall_number": "D-0036-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "69298",
      "termination_date": "20170329",
      "more_code_info": "",
      "recall_initiation_date": "20140926",
      "postal_code": "63045-1220",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}