{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92798",
      "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": "Worldwide distribution - US Nationwide (there was government and military distribution) and the countries of Australia and Singapore.",
      "recall_number": "Z-2657-2023",
      "product_description": "Restore  Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.",
      "product_quantity": "2,408 devices",
      "reason_for_recall": "The original version of the A71100 Restore Clinician Programmer Application has been identified to have a compatibility issue with some legacy clinician programmer software resulting in the programmer having an inability to establish communication with the implanted neurostimulators.",
      "recall_initiation_date": "20200717",
      "center_classification_date": "20230929",
      "termination_date": "20240927",
      "report_date": "20231011",
      "code_info": "Version 1.0.4232, UDI-DI 00763000273668."
    }
  ]
}