{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Belgrade",
      "state": "MT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89367",
      "recalling_firm": "XTANT Medical",
      "address_1": "664 Cruiser Ln",
      "address_2": "N/A",
      "postal_code": "59714-9719",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, MI, NV, and TX   O.U.S.: Portugal",
      "recall_number": "Z-0533-2022",
      "product_description": "X060-0270, 8mm Titanium Insert, Axle Interspinous Fusion System.",
      "product_quantity": "24 devices",
      "reason_for_recall": "The proximal opening of the inserts exhibit an out of specification condition which would prevent the crossbar plates from appropriately engaging with the insert.",
      "recall_initiation_date": "20211229",
      "center_classification_date": "20220128",
      "termination_date": "20240617",
      "report_date": "20220209",
      "code_info": "X060-0270,  8mm Titanium Insert, Axle System UDI (Primary DI Number): M697X06002701/$$7058963W Lot Number: 058963"
    }
  ]
}