{
  "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": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "1266 Kifer Rd Bldg 100",
      "reason_for_recall": "The storage conditions for indocyanine green (ICG) are not on the individual Fluorescence Imaging Procedure Kit box, the six-kit box, and the shipping box.   If heat were to damage the material, the result would be a loss of fluorescence.",
      "address_2": "",
      "product_quantity": "1532 total both devices",
      "code_info": "PN 950156-01",
      "center_classification_date": "20141219",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "CA",
      "product_description": "Fluorescence Imaging Procedure Kit, designed  for use with Firefly Fluorescence Imaging for the da Vinci Si 3000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.",
      "report_date": "20141231",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Intuitive Surgical, Inc.",
      "recall_number": "Z-0834-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69845",
      "termination_date": "20150220",
      "more_code_info": "",
      "recall_initiation_date": "20141121",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}