{
  "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": "Vernon Hills",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74465",
      "recalling_firm": "Carefusion 2200 Inc",
      "address_1": "75 N Fairway Dr",
      "address_2": "N/A",
      "postal_code": "60061-1845",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US, including the states of WA and MD; and, the country of Japan.",
      "recall_number": "Z-2212-2016",
      "product_description": "DIAMOND-FLEX CIRCULAR RETRACTOR, ANGLED, 40MM 5MM, Product Code 89-6114, Lot Code(s): 878971; 879366; 879404, and Date Code:  C16.    Designed to retract or elevate organs and tissue to provide better visualization access.",
      "product_quantity": "10",
      "reason_for_recall": "BD, formerly CareFusion, has identified a potential risk associated with a weld failure which could result in the wire protruding thru the tip of the instrument when articulated. If this failure were to occur while in use in a procedure it has the potential to damages tissue or organs",
      "recall_initiation_date": "20160701",
      "center_classification_date": "20160722",
      "termination_date": "20170329",
      "report_date": "20160803",
      "code_info": "Product Code 89-6114, Lot Code(s): 878971; 879366; 879404, and Date Code:  C16"
    }
  ]
}