{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Minneapolis",
      "address_1": "7000 Central Ave Ne",
      "reason_for_recall": "Medtronic has determined that an Ascenda catheter kit may have had endotoxin in excess of USP limits.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "N457062003",
      "center_classification_date": "20140604",
      "distribution_pattern": "Distributed in the state of CT.",
      "state": "MN",
      "product_description": "Medtronic Model 8780 Ascenda Intrathecal Catheter.    The implantable Medtronic Model 8780 Ascenda Intrathecal Catheter is part of an infusion system that stores and delivers parenteral drugs to the intrathecal space. The implanted infusion system components consist of a Medtronic pump and a Model 8780 Ascenda Intrathecal Catheter.",
      "report_date": "20140611",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Neuromodulation",
      "recall_number": "Z-1723-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68295",
      "termination_date": "20141007",
      "more_code_info": "",
      "recall_initiation_date": "20140502",
      "postal_code": "55432-3568",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}