{
  "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": [
    {
      "status": "Terminated",
      "city": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89983",
      "recalling_firm": "restor3d Inc.",
      "address_1": "311 W Corporation St",
      "address_2": "N/A",
      "postal_code": "27701-2409",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of KY, NC, NJ, TX, IN, VA and AL.",
      "recall_number": "Z-1026-2022",
      "product_description": "Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument",
      "product_quantity": "14 units",
      "reason_for_recall": "Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.",
      "recall_initiation_date": "20220330",
      "center_classification_date": "20220429",
      "termination_date": "20230828",
      "report_date": "20220511",
      "code_info": "Model: 6110-N01-KTS01 Lot: 2022030005 UDI: 00840097504506"
    }
  ]
}