{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Goteborg",
      "state": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90679",
      "recalling_firm": "Nobel Biocare",
      "address_1": "Vastra Hamngatan 1",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S Nationwide.: AZ, CA, CT, FL, HI, NC, NY, OR, PA, TX, UT, and WI  O.U.S.: Austria, Belgium, Canada, Germany, Spain, France, United Kingdom, Hungary, Iceland,  Italy, Netherlands, Norway, Portugal, and Sweden",
      "recall_number": "Z-1565-2022",
      "product_description": "Nobel Biocare N1 TiUltra TCC NP 3.5x13mm",
      "product_quantity": "347 devices",
      "reason_for_recall": "Due to the presence of a burr which may cause an aspiration risk to patient during surgical procedure.",
      "recall_initiation_date": "20220725",
      "center_classification_date": "20220823",
      "report_date": "20220831",
      "code_info": "Catalog number: 300859  Lot numbers / UDI Codes:  12167337 / (01)07332747161717(10)12167337(11)210119(17)251218  12167830 / (01)07332747161717(10)12167830(11)210125(17)251224  12168184 / (01)07332747161717(10)12168184(11)210128(17)251227",
      "more_code_info": ""
    }
  ]
}