{
  "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": "2026-04-01",
    "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": "83503",
      "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": "Updated information provided on 03/18/2020: FL, OH, TN, NJ, PA, MD, NY, CA, MN, NV, OR, HI, VA, TX, AL, CA, IL, CN, and NC.    OUS: APAC (Asia Pacific) - South Korea",
      "recall_number": "Z-1906-2020",
      "product_description": "da Vinci SP Instrument Arm Drape. REF 430013-12  QTY 1 Pouch",
      "product_quantity": "1818 pouches",
      "reason_for_recall": "The instrument drape may tear while draping the Patient Side Cart presenting a breach in the sterile barrier.",
      "recall_initiation_date": "20181025",
      "center_classification_date": "20200506",
      "termination_date": "20240405",
      "report_date": "20200513",
      "code_info": "Model Number: 430013-12  UDI Number: 00886874113486  Lot Numbers:  All Lots",
      "more_code_info": ""
    }
  ]
}