{
  "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": "87481",
      "recalling_firm": "Arthrex, Inc.",
      "address_1": "1370 Creekside Blvd",
      "address_2": "",
      "postal_code": "34108-1945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.",
      "recall_number": "Z-1310-2021",
      "product_description": "Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.",
      "product_quantity": "9 units",
      "reason_for_recall": "The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.",
      "recall_initiation_date": "20210224",
      "center_classification_date": "20210326",
      "termination_date": "20230502",
      "report_date": "20210407",
      "code_info": "Product Code AR-8770-02, Lot Number 032052",
      "more_code_info": ""
    }
  ]
}