{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78315",
      "recalling_firm": "Monteris Medical Corp",
      "address_1": "14755 27th Ave N Ste C",
      "address_2": "N/A",
      "postal_code": "55447-4866",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Canada",
      "recall_number": "Z-0194-2018",
      "product_description": "MONTERIS MEDICAL NEUROBLATE SYSTEM, used for  MRI-guided neurosurgical ablation.",
      "product_quantity": "52 systems",
      "reason_for_recall": "The firm received complaints that involved an unanticipated interaction between a NeuroBlate system and 1.5 Tesla (1.ST) MRI systems.",
      "recall_initiation_date": "20171005",
      "center_classification_date": "20180320",
      "termination_date": "20210121",
      "report_date": "20180328",
      "code_info": "All serial numbers"
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}