{
  "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": "Terminated",
      "city": "Athens",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76292",
      "recalling_firm": "Argon Medical Devices, Inc",
      "address_1": "1445 Flat Creek Rd",
      "address_2": "N/A",
      "postal_code": "75751-5002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and Internationally to Switzerland, Canada, Australia, New Zealand, Ecuador, Colombia, and Japan.",
      "recall_number": "Z-1196-2017",
      "product_description": "HARVEST NEEDLE 15GA X 2    Intended for the purpose of harvesting bone and/or bone marrow specimens",
      "product_quantity": "15 boxes",
      "reason_for_recall": "The recalling firm received a complaint from one of their customers of a potential defect in the forming of  the primary package of the blister that may compromise the sterility of the product inside the tray.",
      "recall_initiation_date": "20170118",
      "center_classification_date": "20170213",
      "termination_date": "20170517",
      "report_date": "20170222",
      "code_info": "lots: 11158857",
      "more_code_info": ""
    }
  ]
}