{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Addison",
      "address_1": "4550 Excel Pkwy Ste 300",
      "reason_for_recall": "Reports received of the device fracturing during insertion.",
      "address_2": "",
      "product_quantity": "46 units",
      "code_info": "Lot numbers 14LEDOEB, 15CNDOHC, and 15DJDOHC.",
      "center_classification_date": "20200704",
      "distribution_pattern": "Distribution was made to AZ, FL, IN, KS, MA, MI, NY, TN, and TX.",
      "state": "TX",
      "product_description": "CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H8mm, Part #018.1908.",
      "report_date": "20200715",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CTL Medical Corporation",
      "recall_number": "Z-2504-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "85218",
      "more_code_info": "",
      "recall_initiation_date": "20190821",
      "postal_code": "75001-5714",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Completed"
    }
  ]
}