{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Asheville",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80601",
      "recalling_firm": "King Bio Inc.",
      "address_1": "3 Westside Dr",
      "address_2": "N/A",
      "postal_code": "28806-2846",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "U.S.A. Nationwide, Canada, and Australia.",
      "recall_number": "D-0966-2019",
      "product_description": "Dr. King's Natural Medicine Regional Allergies Canadian Prairies, 59 mL (liquid/liquide), DIN-HM 80074815 UPC 357955181729",
      "product_quantity": "710 bottles",
      "reason_for_recall": "Microbial contamination",
      "recall_initiation_date": "20180720",
      "center_classification_date": "20190308",
      "termination_date": "20220119",
      "report_date": "20190320",
      "code_info": "Lot: 021517L Exp. 02/20"
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}