{
  "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": "2026-04-08",
    "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": "84023",
      "recalling_firm": "Intuitive Surgical, Inc.",
      "address_1": "1266 Kifer Rd Bldg 101",
      "address_2": "N/A",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, MD, NY, VA, IL, MI, DE, TX, FL, NJ, MA, KY and OH.    O.U.S.: Australia, France, Germany and Japan.",
      "recall_number": "Z-1960-2020",
      "product_description": "da Vinci Xi Surgical System",
      "product_quantity": "74 USMs containing affected rotors.",
      "reason_for_recall": "Due to a manufacturing variation in the arm that can result in a persistent recoverable fault error (error 23087) and loss of arm functionality prior or during surgery.",
      "recall_initiation_date": "20181121",
      "center_classification_date": "20200511",
      "termination_date": "20220531",
      "report_date": "20200520",
      "code_info": "Model: IS4000  UDI: 00886874114216  Device Listing: D215864    For System Name and USM Serial Numbers, refer to:  ISIFA2018-15-C 806.10 Report_Affected Products List - Copy\" files in Associated Documents."
    }
  ]
}