{
  "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": "2026-04-08",
    "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": "79749",
      "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": "USA (nationwide) Distribution and Internationally to Turkey.",
      "recall_number": "Z-1485-2018",
      "product_description": "Genesis Surgical Cassette Tapered      Implants are intended for placement following natural tooth loss or for immediate placement into an extraction socket",
      "product_quantity": "19",
      "reason_for_recall": "The surgical cassette contained extra-large white grommets making the 3.8 mm and 6.5mm dental burrs  wobble  within the grommets in the surgical cassette.",
      "recall_initiation_date": "20180313",
      "center_classification_date": "20180424",
      "termination_date": "20180723",
      "report_date": "20180502",
      "code_info": "lot #s  38177  38330  38421"
    }
  ]
}