{
  "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": "88917",
      "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": "US Nationwide distribution.",
      "recall_number": "Z-0203-2022",
      "product_description": "GM Helix Acqua Implant 3.5x10, Article No. 140.944",
      "product_quantity": "567 (US)",
      "reason_for_recall": "3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline cases where the bone quality is low and the bone ridge has a maximum indication for the implant height (10mm), if the incorrect implant is installed, it could result in damage to the nerve or adjacent bone structures/cavities.",
      "recall_initiation_date": "20211011",
      "center_classification_date": "20211104",
      "termination_date": "20240116",
      "report_date": "20211110",
      "code_info": "UDI 7899878024897  Lots GNW15 and GRE82"
    }
  ]
}