{
  "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": "Bergen",
      "state": "N/A",
      "country": "Norway",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80529",
      "recalling_firm": "NordicNeuroLab AS",
      "address_1": "Mollendalsveien 65c",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "worldwide",
      "recall_number": "Z-3023-2018",
      "product_description": "fMRI Hardware System   VisualSystem allows video signals from the stimulus presentation PC to enter the shielded scanner room and presented by a set of coil-mounted displays or by an in-room LCD monitor.  - LCD Monitor Power supply (LPS) for LCD Monitor, Versions 1.0 and 1.1",
      "product_quantity": "163 units",
      "reason_for_recall": "Complaints of this version of the power supply unit (LPS) (1.0 and 1.1) being dragged into the magnet bore (MR Scanner).",
      "recall_initiation_date": "20180820",
      "center_classification_date": "20180911",
      "termination_date": "20200916",
      "report_date": "20180919",
      "code_info": "Serial numbers:    LPS-2011-1.0-XXX   LPS-2012-1.0-XXX   LPS-2012-1.1-XXX   LPS-2013-1.1-XXX"
    }
  ]
}