{
  "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 100",
      "reason_for_recall": "An increase in the number of da Vinci EndoWrist Stapler complaints where the customer experienced a  Stapler Firing Failed message as well as review of da Vinci Xi Surgical System logs found an increased trend",
      "address_2": "",
      "product_quantity": "2065  total",
      "code_info": "All",
      "center_classification_date": "20160805",
      "distribution_pattern": "US, including Puerto Rico and Australia, Austria, Belgium, Chile, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, Ireland, Italy, Japan, Monaco, Netherlands, Norway, Portugal, , Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Kingdom, Venezuela.",
      "state": "CA",
      "product_description": "STAPLER 30, IS4000, model number 470430;    Gastroenterology/Urology: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection and/or creation of  anastomoses in General, Thoracic, Gynecologic, and Urologic surgery. The device is indicated for adult and pediatric use. The device can be used with staple line or tissue buttressing material.",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Intuitive Surgical, Inc.",
      "recall_number": "Z-2349-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74705",
      "termination_date": "20170103",
      "more_code_info": "",
      "recall_initiation_date": "20160714",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}