{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74583",
      "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": "Distributed in the US to the states of FL, VA, OK, CO, DC, and IN.",
      "recall_number": "Z-2296-2016",
      "product_description": "Integra External Fixation System Rocker Bottom Model # 12225400.    For use in the treatment of bone conditions amenable to treatment by the use of external fixation.",
      "product_quantity": "27 units",
      "reason_for_recall": "The silicone insert embedded in the rocker bottom has the potential to become dislodged or loose from the rocker bottom mold.",
      "recall_initiation_date": "20160701",
      "center_classification_date": "20160727",
      "termination_date": "20161216",
      "report_date": "20160803",
      "code_info": "Lot # PN625."
    }
  ]
}