{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65999",
      "recalling_firm": "Spine Smith Holdings, LLC",
      "address_1": "93 Red River St",
      "address_2": "N/A",
      "postal_code": "78701-4216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "Distributed in FL.",
      "recall_number": "Z-2258-2013",
      "product_description": "VisuALIF,System consisting of a 'U' shaped PEEK block in two footprint configurations, four heights and three lordosis angles., part number:  0301-1410.    Intended to be implanted via an open anterior approach.",
      "product_quantity": "32",
      "reason_for_recall": "The product has the potential to be laser marked as a Medium when it actually is a Small.",
      "recall_initiation_date": "20130731",
      "center_classification_date": "20130919",
      "termination_date": "20140318",
      "report_date": "20130925",
      "code_info": "Part Number:  0301-1410, Lot 53AR",
      "more_code_info": ""
    }
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}