{
  "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": "Ongoing",
      "city": "Charlotte",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82045",
      "recalling_firm": "KaVo Dental Technologies LLC",
      "address_1": "11727 Fruehauf Dr",
      "address_2": "N/A",
      "postal_code": "28273-6507",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution in NC",
      "recall_number": "Z-1101-2019",
      "product_description": "cone-beam CT system",
      "product_quantity": "230",
      "reason_for_recall": "ORTHOPANTOMOGRAPH OP 3D device has a  defect in the device firmware versions 2.1.0 and 2.1.1",
      "recall_initiation_date": "20181231",
      "center_classification_date": "20190422",
      "report_date": "20190501",
      "code_info": "versions 2.1.0 and 2.1.1"
    }
  ]
}