{
  "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": "73426",
      "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": "Internationally to Japan.",
      "recall_number": "Z-1271-2016",
      "product_description": "Medtronic, Model 8781 Ascenda\" Intrathecal Catheter kit, Rx Only, Sterile Ethylene Oxide.",
      "product_quantity": "9 (1 still unused)",
      "reason_for_recall": "Medtronic Neuromodulation is initiating a voluntary removal of a single Model 8781 Ascenda\" Intrathecal Catheter kit.  We have identified that this kit may have been produced with incorrect outer package labels.  As a result, it may not contain all components necessary to complete the implant procedure.",
      "recall_initiation_date": "20160209",
      "center_classification_date": "20160329",
      "termination_date": "20160811",
      "report_date": "20160406",
      "code_info": "N558983006"
    }
  ]
}