{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Belgrade",
      "state": "MT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95395",
      "recalling_firm": "XTANT Medical Holdings, Inc",
      "address_1": "664 Cruiser Ln",
      "address_2": "",
      "postal_code": "59714-9719",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of IL, WI, FL, PA, CA, TX, MI, MO, VA, OH, MA.",
      "recall_number": "Z-0125-2025",
      "product_description": "Cortera Spinal Fixation System Screw, Poly, Solid, 6.5mm x 45mm, REF: 150100-65045",
      "product_quantity": "330",
      "reason_for_recall": "Spinal fixation system implant screws marked \"DNI\" are not intended to be implanted and may not have been manufactured in accordance with released manufacturing specifications, and if implanted the screws may not have adequate strength or performance.",
      "recall_initiation_date": "20240821",
      "center_classification_date": "20241017",
      "report_date": "20241023",
      "code_info": "UDI-DI: 00810076563190, Lot: DNI",
      "more_code_info": ""
    }
  ]
}