{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Daytona Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80750",
      "recalling_firm": "Product Quest Manufacturing LLC",
      "address_1": "330 Carswell Ave",
      "address_2": "N/A",
      "postal_code": "32117-4416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0066-2019",
      "product_description": "FREEZE IT (camphor 0.2% and menthol 3.5%) spray, 118.29 mL (4 fl. oz.) can, Distributed by: Expedite Products, Inc., Tampa, FL 33619 USA, UPC 8 56569 00203 6.",
      "product_quantity": "6,109 cans",
      "reason_for_recall": "Superpotent Drug: high out of specification assay results for the camphor ingredient.",
      "recall_initiation_date": "20180803",
      "center_classification_date": "20181016",
      "termination_date": "20210330",
      "report_date": "20181024",
      "code_info": "Lot: 170498B, Exp. 02/23/2020"
    }
  ]
}