{
  "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": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "1266 Kifer Rd Bldg 101",
      "reason_for_recall": "An Endoscope Controller has been improperly calibrated during manufacturing. This improper calibration may result in the Endoscope Controller showing surgical images that are dimmer, have color imbalance or have reduced fluorescence and grayscale when using Firefly. There is also potential for increased fogging of the endoscope.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "UDI Number: 00886874114193.  Serial Number: SK1703.",
      "center_classification_date": "20180816",
      "distribution_pattern": "U.S.",
      "state": "CA",
      "product_description": "The da Vinci Xi Surgical System (IS4000) Model Name: IS4000, Endoscope Controller.  Model Number:   372601-16.",
      "report_date": "20180822",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Intuitive Surgical, Inc.",
      "recall_number": "Z-2835-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80691",
      "more_code_info": "",
      "recall_initiation_date": "20180517",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}