{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Winter Park",
      "address_1": "1300 Minnesota Ave",
      "reason_for_recall": "The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to initial product marketing.",
      "address_2": "Suite 200",
      "product_quantity": "400",
      "code_info": "Ref. No. CL1012-05   Size  10mm x 12mm x 5mm,  Ref. No. CL1012-06   Size 10mm x 12mm x 6mm,  Ref. No. CL1012-07   Size 10mm x 12mm x 7mm,  Ref. No. CL1012-08   Size 10mm x 12mm x 8mm,  Ref. No. CL1012-09   Size 10mm x 12mm x 9mm,  Ref. No. CL1012-10   Size 10mm x 12mm x 10mm,  Ref. No. CL1014-05   Size 12mm x 14mm x 5mm,  Ref. No. CL1014-06   Size 12mm x 14mm x 6mm,  Ref. No. CL1014-07   Size 12mm x 14mm x 7mm,  Ref. No. CL1014-08   Size 12mm x 14mm x 8mm,  Ref. No. CL1014-09   Size 12mm x 14mm x 9mm, and  Ref. No. CL1014-10   Size 12mm x 14mm x 10mm.",
      "center_classification_date": "20130827",
      "distribution_pattern": "USA Nationwide Distribution in the state of Florida",
      "state": "FL",
      "product_description": "SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage)    Product Usage:  Is indicated for use in skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SpineNet",
      "recall_number": "Z-2103-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65917",
      "termination_date": "20140502",
      "more_code_info": "",
      "recall_initiation_date": "20130205",
      "postal_code": "32789-4800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}