{
  "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": "Westlake Village",
      "address_1": "3050 E Hillcrest Dr",
      "reason_for_recall": "Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour Abutment 3.5mmD Assembly because it may be out of Implant Direct specification.",
      "address_2": "",
      "product_quantity": "151 units",
      "code_info": "89103, 83493, 78986",
      "center_classification_date": "20170522",
      "distribution_pattern": "Worldwide Distribution - Nationwide Distribution  and to the countries of : European Union (HU, GB, DE, DK, IT, HR, FR), and  Japan",
      "state": "CA",
      "product_description": "Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Implant Direct Sybron Manufacturing, LLC",
      "recall_number": "Z-2125-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77171",
      "termination_date": "20180108",
      "more_code_info": "",
      "recall_initiation_date": "20170502",
      "postal_code": "91362-3171",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}