{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Belgrade",
      "address_1": "664 Cruiser Ln",
      "reason_for_recall": "The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.",
      "address_2": "",
      "product_quantity": "4 units",
      "code_info": "LOT: XS1920458A",
      "center_classification_date": "20200704",
      "distribution_pattern": "AZ, TX and WV.",
      "state": "MT",
      "product_description": "Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591",
      "report_date": "20200715",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "XTANT Medical",
      "recall_number": "Z-2500-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85789",
      "termination_date": "20210319",
      "more_code_info": "",
      "recall_initiation_date": "20200512",
      "postal_code": "59714-9719",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}