{
  "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": "Mcminnville",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71344",
      "recalling_firm": "Vilex In Tennessee Inc",
      "address_1": "111 Moffitt Street",
      "address_2": "N/A",
      "postal_code": "37110-2235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distributed in the states of MS, MD, PA, and TX.",
      "recall_number": "Z-1722-2015",
      "product_description": "Vilex, Inc., FUZE 10.0 mm x 200 mm, Product # FZ100-200T-25.    Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.",
      "product_quantity": "7 units",
      "reason_for_recall": "Incidence of breakage is higher than expected.",
      "recall_initiation_date": "20150422",
      "center_classification_date": "20150608",
      "termination_date": "20161030",
      "report_date": "20150617",
      "code_info": "all codes"
    }
  ]
}