{
  "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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      "limit": 1,
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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-0858-2019",
      "product_description": "Dr. King's SafeCare Rx Menopause Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000624, NDC 57955-0006-2",
      "product_quantity": "753 bottles",
      "reason_for_recall": "Microbial contamination",
      "recall_initiation_date": "20180720",
      "center_classification_date": "20190308",
      "termination_date": "20220119",
      "report_date": "20190320",
      "code_info": "Lots: 072815C Exp. 07/18; 092216M Exp. 09/19"
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