{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Earth City",
      "address_1": "13600 Shoreline Dr",
      "reason_for_recall": "Failed Dissolution Specifications: Drug failed stage III dissolution testing.",
      "address_2": "",
      "product_quantity": "92,544 Bottles",
      "code_info": "Lot # A308879, Expiry: 09/2015",
      "center_classification_date": "20140630",
      "distribution_pattern": "Nationwide including Puerto Rico.",
      "state": "MO",
      "product_description": "Bystolic (nebivolol) tablets, 20 mg/tablet. 7 Tablet Professional Sample Bottle, Rx Only.  Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, Missouri 63045. NDC 0456-1420-07.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Forest Pharmaceuticals Inc",
      "recall_number": "D-1412-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "68548",
      "termination_date": "20160105",
      "more_code_info": "",
      "recall_initiation_date": "20140619",
      "postal_code": "63045",
      "voluntary_mandated": "Voluntary: Firm initiated",
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