{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Burlington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64477",
      "recalling_firm": "Keystone Dental Inc",
      "address_1": "144 Middlesex Tpke",
      "address_2": "N/A",
      "postal_code": "01803-4403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "FAX",
      "distribution_pattern": "Nationwide Distribution including CA, IN, MA, MD, MN, MI, , NH, NY, NC, PA, and WI.",
      "recall_number": "Z-0923-2013",
      "product_description": "Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment  Part Number: G71200    Genesis implant for single stage or two stage surgical procedures all types of of bone in partially or fully edentulous mandibles and maxillae.",
      "product_quantity": "35 units",
      "reason_for_recall": "Mislabeled: Genesis Straight Esthetic 5.0mm Contour ,3mm cuff labeled as Genesis Straight Esthetic 4.0 mm, 1 mm cuff abutment,",
      "recall_initiation_date": "20110705",
      "center_classification_date": "20130308",
      "termination_date": "20130311",
      "report_date": "20130320",
      "code_info": "Lot Number: 2376  Exp Date: 09/2013",
      "more_code_info": ""
    }
  ]
}