{
  "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": [
    {
      "country": "United States",
      "city": "Minneapolis",
      "address_1": "7000 Central Ave",
      "reason_for_recall": "Medtronic has voluntarily decided to retrieve unused Model 3387S-40 and 3389S-40 DBS leads from three manufacturing lot numbers.  During the manufacturing process of a DBS lead component, Medtronic identified the potential for lead insulation damage.",
      "address_2": "",
      "product_quantity": "70",
      "code_info": "lots: VA15GPJ, VA15K3N, VA15K7K",
      "center_classification_date": "20160819",
      "distribution_pattern": "US: AR, CA, FL, IL MD, MO, NE, NY, OH, TN WI.",
      "state": "MN",
      "product_description": "Medtronic, Lead Kit for DBS Stimulation. Model Numbers 3387S-40 (p/n 3387S0007V) & 3389S-40 (p/n 3389S0008V).",
      "report_date": "20160831",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Neuromodulation",
      "recall_number": "Z-2602-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74545",
      "termination_date": "20161003",
      "more_code_info": "",
      "recall_initiation_date": "20160610",
      "postal_code": "55421-1241",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}