{
  "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": [
    {
      "country": "United States",
      "city": "Carlsbad",
      "address_1": "3115 Melrose Dr",
      "reason_for_recall": "Spinal Elements is recalling the Ti-Bond related brochures that includes LT-10000 and MP-14000 (all revisions) the content regarding the Ti-Bond coating within the literature is unsubstantiated in context and/or misleading for the coating's use in spine applications.",
      "address_2": "Suite 200",
      "product_quantity": "1200 units",
      "code_info": "All revisions",
      "center_classification_date": "20150105",
      "distribution_pattern": "Nationwide Distribution",
      "state": "CA",
      "product_description": "Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000  This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.",
      "report_date": "20150114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Spinal Elements, Inc",
      "recall_number": "Z-0907-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70044",
      "termination_date": "20150310",
      "more_code_info": "",
      "recall_initiation_date": "20141218",
      "postal_code": "92010-6690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}