{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75068",
      "recalling_firm": "LDR Spine USA, Inc.",
      "address_1": "13785 Research Blvd Ste 200",
      "address_2": "N/A",
      "postal_code": "78750-1895",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to states of: GA, OR, FL, KY, NC, AR and PA.",
      "recall_number": "Z-0045-2017",
      "product_description": "ROI-A Anterior Delivery Device.  Orthopedic manual surgical instrument. Model number: SI-ROIA-0023    Auxiliary instrument used in the ROI-A-ALIR cage system: Spinal intervertbral body fusion device.",
      "product_quantity": "24 units",
      "reason_for_recall": "The ROI-A Anterior Delivery Device T-Handle, part number SI-ROIA-0023 has experienced binding of the rotation of the t-handle.  There have been no reports of patient injury",
      "recall_initiation_date": "20160829",
      "center_classification_date": "20161005",
      "termination_date": "20170113",
      "report_date": "20161012",
      "code_info": "Lot # 2295101A, 2295101A-R, 2296101A-R"
    }
  ]
}