{
  "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": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80667",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 NW 66th Ct",
      "address_2": "N/A",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "CA, OH, NY, OK, FL, TX, SC, Germany, Spain, Switzerland, and UK",
      "recall_number": "Z-2966-2018",
      "product_description": "Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.",
      "product_quantity": "7 units",
      "reason_for_recall": "Exactech is recalling the Tibial Alignment Guide because the Global Trade Item Number (GTIN) on the device is incorrect.  The GTIN on the device reads 10885862525629, when it should read 10885862525628.",
      "recall_initiation_date": "20180713",
      "center_classification_date": "20180831",
      "termination_date": "20210422",
      "report_date": "20180912",
      "code_info": "GTIN10885862525629, Lot Number 098299003"
    }
  ]
}