{
  "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": {
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    }
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  "results": [
    {
      "status": "Terminated",
      "city": "Oslo",
      "state": "N/A",
      "country": "Norway",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78973",
      "recalling_firm": "Medistim Asa",
      "address_1": "Okernveien 94",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distributed to New York.",
      "recall_number": "Z-0719-2018",
      "product_description": "MEDISTIM VERIQ SYSTEM, MODEL VQ4122    An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.",
      "product_quantity": "2",
      "reason_for_recall": "A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.",
      "recall_initiation_date": "20170425",
      "center_classification_date": "20180226",
      "termination_date": "20240503",
      "report_date": "20180307",
      "code_info": "UDI: 7070554101198  Serial#: 1170 and 1294"
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}