{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Naples",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84594",
      "recalling_firm": "Arthrex, Inc.",
      "address_1": "1370 Creekside Blvd",
      "address_2": "N/A",
      "postal_code": "34108-1945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide in US; no distribution OUS.",
      "recall_number": "Z-0919-2020",
      "product_description": "Arthrex Fibulock Fibular Nail Instrument Set  Reusable non-sterile instruments  Outrigger Targeting Guide",
      "product_quantity": "47",
      "reason_for_recall": "There is a potential for blockage of the Hub Attachment Tube.",
      "recall_initiation_date": "20191217",
      "center_classification_date": "20200130",
      "termination_date": "20230831",
      "report_date": "20200205",
      "code_info": "Batch/Lot 051838"
    }
  ]
}