{
  "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": "Santa Clarita",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80184",
      "recalling_firm": "Shadow Holdings DBA Bocchi Labs",
      "address_1": "26421 Ruether Ave",
      "address_2": "N/A",
      "postal_code": "91350-2621",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0858-2018",
      "product_description": "X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottles (UPC 8 50547 00503 3, Distributed by Herb-X Solutions, Inc., 3838 West Burbank Blvd., Burbank CA 91505.",
      "product_quantity": "12,252 bottles",
      "reason_for_recall": "CGMP Deviations: products may be contaminated with bacteria.",
      "recall_initiation_date": "20180525",
      "center_classification_date": "20180612",
      "termination_date": "20190813",
      "report_date": "20180620",
      "code_info": "All lots"
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}