{
  "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": "Burlington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80112",
      "recalling_firm": "Keystone Dental Inc",
      "address_1": "154 Middlesex Tpke",
      "address_2": "N/A",
      "postal_code": "01803-4403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of :  CA, CT, FL, IN, MA, MD, MI, MN, MT, NJ, NV, NY, TX, and VA.",
      "recall_number": "Z-2162-2018",
      "product_description": "Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K    Keystone Dental implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations including cement retained, or overdenture restorations, and terminal or intermediate abutment support for fixed bridgework.",
      "product_quantity": "72",
      "reason_for_recall": "The implants are mislabeled.",
      "recall_initiation_date": "20180501",
      "center_classification_date": "20180611",
      "termination_date": "20180914",
      "report_date": "20180620",
      "code_info": "UDI: D76815737K0, Lot 37038"
    }
  ]
}