{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Hendersonville",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84117",
      "recalling_firm": "Basic Reset Inc.",
      "address_1": "260 W Main St Ste 103",
      "address_2": "N/A",
      "postal_code": "37075-7316",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US, Puerto Rico, U.S. Virgin Islands,  Canada, Mexico, Australia, PHILIPPINES,  Greece, United Kingdom, Israel, Nigeria, Hungary, United Arab Emirates",
      "recall_number": "Z-0348-2020",
      "product_description": "Energy FX:  a) original Aluminum (100-3A)   b) sleek (adult and kid & pet) (100-3B)",
      "product_quantity": "1257 units",
      "reason_for_recall": "FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.",
      "recall_initiation_date": "20191018",
      "center_classification_date": "20191108",
      "report_date": "20191120",
      "code_info": "All product distributed between November 7, 2017 to September 4, 2019"
    }
  ]
}