{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92530",
      "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": "Visit",
      "distribution_pattern": "International distribution to the countries of Israel and Serbia.",
      "recall_number": "Z-2226-2023",
      "product_description": "A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..",
      "product_quantity": "2 clinician tablets",
      "reason_for_recall": "When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.",
      "recall_initiation_date": "20230621",
      "center_classification_date": "20230721",
      "report_date": "20230802",
      "code_info": "Serial numbers NPL3011706 and NPL3016791, UDI-DI 643169738058."
    }
  ]
}