{
  "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": "2026-04-08",
    "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": "87674",
      "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.",
      "recall_number": "Z-1535-2021",
      "product_description": "Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargeable neurostimulators: \u001c Intellis with AdaptiveStim Technology Model 97715 Implanted Neurostimulator \u001c Intellis Model 97716 Implanted Neurostimulator.",
      "product_quantity": "79,616 units",
      "reason_for_recall": "There is a potential for unintended heating that can occur with the Intellis Model 97755 Recharger.",
      "recall_initiation_date": "20210325",
      "center_classification_date": "20210506",
      "report_date": "20210512",
      "code_info": "All serial numbers"
    }
  ]
}