{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Carlsbad",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98967",
      "recalling_firm": "Alphatec Spine, Inc.",
      "address_1": "1950 Camino Vida Roble",
      "address_2": "N/A",
      "postal_code": "92008-6505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of TX, MO, IN.",
      "recall_number": "Z-2793-2026",
      "product_description": "SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System",
      "product_quantity": "3",
      "reason_for_recall": "Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, and prompts requiring system reboot; may result in increased operative time and surgical plan change.",
      "recall_initiation_date": "20260513",
      "center_classification_date": "20260723",
      "report_date": "20260729",
      "code_info": "UDI-DI: 00190376517506. System Set ID/Patient Interface Serial Number: 2007716/ DG106225, 2005498/ DG106220, 2005490/ DG106230"
    }
  ]
}