{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Miramar Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69053",
      "recalling_firm": "Baro-Therapies, Inc",
      "address_1": "80 S Geronimo St",
      "address_2": "Unit 3",
      "postal_code": "32550-8035",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of FL, GA, MS, TN and CO.",
      "recall_number": "Z-2734-2014",
      "product_description": "The Rejuvenator Chamber manufactured by Baro-Therapies, Inc.    Product  Usage:  Indicated for relief from general aches and pains brought on by changes in the weather.",
      "product_quantity": "10",
      "reason_for_recall": "The firm is distributing the Rejuvenator device without an approved 510(k).",
      "recall_initiation_date": "20140808",
      "center_classification_date": "20140930",
      "termination_date": "20150806",
      "report_date": "20141008",
      "code_info": "All Lots, Series and Codes"
    }
  ]
}