{
  "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": "2026-04-29",
    "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": "98541",
      "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:  OR",
      "recall_number": "Z-1773-2026",
      "product_description": "XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.",
      "product_quantity": "2 units",
      "reason_for_recall": "Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.",
      "recall_initiation_date": "20260218",
      "center_classification_date": "20260403",
      "report_date": "20260415",
      "code_info": "UDI/DI M697X0736555DL1, Lot Number 4375-01",
      "more_code_info": ""
    }
  ]
}