{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Curitiba",
      "state": "N/A",
      "country": "Brazil",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84709",
      "recalling_firm": "Jjgc Industria E Comercio De Materials Dentarios Sa",
      "address_1": "Av Juscelino Kubitschek De Oliveira",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to consignees in CA and PA.",
      "recall_number": "Z-0924-2020",
      "product_description": "Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.",
      "product_quantity": "2",
      "reason_for_recall": "The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the \"4.3+ Tapered Guided Surgery Drill\".",
      "recall_initiation_date": "20191223",
      "center_classification_date": "20200131",
      "termination_date": "20210601",
      "report_date": "20200212",
      "code_info": "Lot WH723"
    }
  ]
}