{
  "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": [
    {
      "country": "United States",
      "city": "Naples",
      "address_1": "1370 Creekside Blvd",
      "reason_for_recall": "Potential for polystyrene particulate presence.",
      "address_2": "",
      "product_quantity": "138 total products",
      "code_info": "Catalog #: AR-8948W-2065; Batch #: 10019150; Unique Device Identifier: 00888867202757.",
      "center_classification_date": "20160614",
      "distribution_pattern": "Distributed in the states of CA, CO, FL, GA, IL, IN, KS, MD, NC, NY, PA, SC, VA, WA, and WI.",
      "state": "FL",
      "product_description": "BioSync Anatomic Cotton Wedge, 20 x 6.5 mm.; Used for internal bone fixation for bone fractures, fusions or osteotomies in the ankle and foot.",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arthrex, Inc.",
      "recall_number": "Z-1963-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74084",
      "termination_date": "20171013",
      "more_code_info": "",
      "recall_initiation_date": "20160422",
      "postal_code": "34108-1945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}