{
  "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": "2026-04-29",
    "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": "71016",
      "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",
      "recall_number": "Z-1617-2015",
      "product_description": "Medtronic DBS Extension Kit for Deep Brain Stimulation,  Models 37085 and 37086.  Sterile",
      "product_quantity": "86,851 (US 37,933 / OUS 48,918)",
      "reason_for_recall": "Medtronic is providing Important information regarding extension handling during implant procedure after receiving reports of high impedances.  This applies to extension Models 37085 and 37086 which can be used with the following  implantable Neurostimulators: Activa¿ PC (Model 37601), Activa¿ RC (Model 37612), and the Activa¿  SC (Model 37603).",
      "recall_initiation_date": "20150416",
      "center_classification_date": "20150515",
      "termination_date": "20160722",
      "report_date": "20150527",
      "code_info": "all Serial numbers"
    }
  ]
}