{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93419",
      "recalling_firm": "APN Health LLC",
      "address_1": "20935 Swenson Dr Ste 160",
      "address_2": "N/A",
      "postal_code": "53186-2057",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of WI.",
      "recall_number": "Z-0556-2024",
      "product_description": "Navik 3D v2, REF NAVIK3D, 3D Mapping System",
      "product_quantity": "1 unit",
      "reason_for_recall": "IFU update",
      "recall_initiation_date": "20231107",
      "center_classification_date": "20231214",
      "report_date": "20231220",
      "code_info": "UDI (01)00869781000308(11)180309(21)2UA7520XNT"
    }
  ]
}