{
  "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": [
    {
      "country": "United States",
      "city": "Minneapolis",
      "address_1": "7000 Central Ave",
      "reason_for_recall": "Medtronic received a complaint that there was an error code  displayed on the programmer when the physician attempted  to interrogate an implanted SynchroMed II pump. The error  code prevented the physician from updating the pump;  however the pump was providing therapy.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Serial Number NGV526743H",
      "center_classification_date": "20170329",
      "distribution_pattern": "IL",
      "state": "MN",
      "product_description": "SynchroMed II implantable drug infusion pump, Model 8637-40,",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Neuromodulation",
      "recall_number": "Z-1694-2017",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "76591",
      "termination_date": "20180904",
      "more_code_info": "",
      "recall_initiation_date": "20170209",
      "postal_code": "55421-1241",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}