{
  "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": [
    {
      "status": "Terminated",
      "city": "Plainsboro",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76408",
      "recalling_firm": "Integra LifeSciences Corp.",
      "address_1": "311 Enterprise Dr",
      "address_2": "N/A",
      "postal_code": "08536-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1410-2017",
      "product_description": "The UNI-CP System; Model Number: 330230SND.",
      "product_quantity": "39 units",
      "reason_for_recall": "The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.",
      "recall_initiation_date": "20170125",
      "center_classification_date": "20170304",
      "termination_date": "20171108",
      "report_date": "20170315",
      "code_info": "Lot # FEDT"
    }
  ]
}