{
  "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": "Ocala",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70445",
      "recalling_firm": "Biologic Therapies, Inc",
      "address_1": "5817 Nw 44th Ave",
      "address_2": "N/A",
      "postal_code": "34482-7891",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution in states of: MA, CA, WA, NJ, TX, IL, and FL.",
      "recall_number": "Z-1374-2015",
      "product_description": "Bio-CORE Cannula (Needle) Set",
      "product_quantity": "0 (distributed or released)",
      "reason_for_recall": "Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution",
      "recall_initiation_date": "20150123",
      "center_classification_date": "20150402",
      "termination_date": "20150806",
      "report_date": "20150408",
      "code_info": "Catalog Numbers: Part # BCORE.60, BCORE.80, and BCORE.105"
    }
  ]
}