{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sunnyvale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65072",
      "recalling_firm": "Intuitive Surgical, Inc.",
      "address_1": "1266 Kifer Rd Bldg 100",
      "address_2": "N/A",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide distribution",
      "recall_number": "Z-1426-2013",
      "product_description": "Thyroidectomy Indication for the da Vinci Surgical Systems;    Product Usage:  da Vinci Thyroidectomy offers a minimally invasive surgery for both partial and total thyroidectomy procedures, including endoscopic and video assisted procedure that are preferable to conventional (open) procedures that utilize a cervical incision because they leave no visible neck scar.",
      "product_quantity": "2,423 consignee",
      "reason_for_recall": "Promotional literature for use of the da Vinci system for thyroidectomy, which had not been approved with a change to the 510(k).",
      "recall_initiation_date": "20111013",
      "center_classification_date": "20130529",
      "termination_date": "20130530",
      "report_date": "20130605",
      "code_info": "NA - marketing and promotional only."
    }
  ]
}