{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69514",
      "recalling_firm": "Monteris Medical Corp",
      "address_1": "16305 36th Ave N Suite 200",
      "address_2": "N/A",
      "postal_code": "55446-2884",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Distribution including the states of CA, CT, FL, GA, KS, MN, MO, NC, OH, PA, TX, and VA",
      "recall_number": "Z-0227-2015",
      "product_description": "SideFire Directional Laser Probe, REF:  NBP101-01, NBP201-01, NBP301-01, NBP401-01, NBP501-01.  These laser probes are part of the NeuroBlate System, a unique collection of MRI-compatible laser devices and accessories that create an MRI guided delivery of precision thermal therapy in the brain.  The NeuroBlate System components include Gas-cooled Laser Delivery Probes to deliver controlled energy to a target zone.",
      "product_quantity": "234 devices",
      "reason_for_recall": "Monteris Medical received a complaint of a separation of the distal sapphire tip from the laser delivery probe.",
      "recall_initiation_date": "20141003",
      "center_classification_date": "20141119",
      "termination_date": "20141208",
      "report_date": "20141126",
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