{
  "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": "2026-05-06",
    "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": "62993",
      "recalling_firm": "Spine Smith Partners LP",
      "address_1": "93 Red River St",
      "address_2": "N/A",
      "postal_code": "78701-4216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in Texas.",
      "recall_number": "Z-0932-2013",
      "product_description": "Cynch Lordotic T-PLlF Implant.  Intervertebral fusion device with bone graft, for use with supplemental fixation.",
      "product_quantity": "3 units",
      "reason_for_recall": "Implants were incorrectly laser marked as 23mm instead of  28mm.",
      "recall_initiation_date": "20120824",
      "center_classification_date": "20130310",
      "termination_date": "20130517",
      "report_date": "20130320",
      "code_info": "Part Number: 0609-2809-06, Lot: 39AQ",
      "more_code_info": ""
    }
  ]
}