{
  "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": {
      "skip": 0,
      "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-0805-2019",
      "product_description": "Dr. King's SafeCare Rx VeinoPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006626, NDC 57955-0066-2",
      "product_quantity": "245 bottles",
      "reason_for_recall": "Microbial contamination",
      "recall_initiation_date": "20180720",
      "center_classification_date": "20190308",
      "termination_date": "20220119",
      "report_date": "20190320",
      "code_info": "Lots: 062415H Exp. 06/18; 111516P Exp. 11/19; 062016D Exp. 06/19; 040717D Exp. 04/19"
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}