{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93303",
      "recalling_firm": "Medtronic Neuromodulation",
      "address_1": "7000 Central Ave Ne",
      "address_2": "N/A",
      "postal_code": "55432-3568",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution to the countries of S. Korea and Turkey.",
      "recall_number": "Z-0354-2024",
      "product_description": "Model 97745 Controller used with Models 97715 and 97716 Intellis Neurostimulators",
      "product_quantity": "26 units",
      "reason_for_recall": "Units distributed in Korea and Turkey that did not have the correct firmware installed to support the user interface in the local language.",
      "recall_initiation_date": "20231019",
      "center_classification_date": "20231120",
      "report_date": "20231129",
      "code_info": "UDI/DI 00763000642297, Serial Numbers:  NLD172060N, NLD142952N, NLD172064N, NLD142947N, NLD142942N, NLD172061N, NLD172062N, NLD172063N, NLD172066N;  UDI/DI 00763000724436, Serial Numbers:  NLD160337N, NLD163006N, NLD142943N, NLD163007N, NLD142944N, NLD163008N, NLD160338N, NLD163009N, NLD160339N, NLD163010N, NLD160340N, NLD163011N",
      "more_code_info": ""
    }
  ]
}