{
  "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": "2026-04-15",
    "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": "73139",
      "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, including US Nationwide.",
      "recall_number": "Z-0859-2016",
      "product_description": "Specify 5-6-5 Lead, Specify 2x8 Lead, Model Numbers: 39565, 39286.  Spinal cord stimulation leads.  Part of a neurostimulation system for treating chronic, intractable pain of the trunk and/or limbs-including unilateral or bilateral pain.",
      "product_quantity": "51,138 (44,006 US; 9,132 OUS)",
      "reason_for_recall": "Some Specify 5-6-5 and 2x8 surgical lead product labeling does not adequately distinguish between permanent surgical implant and trialing/screening use.",
      "recall_initiation_date": "20160111",
      "center_classification_date": "20160223",
      "termination_date": "20170120",
      "report_date": "20160302",
      "code_info": "All lot/serial numbers are affected for both Model numbers: 39565 and 39286",
      "more_code_info": ""
    }
  ]
}