{
  "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": "2026-04-29",
    "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": "65094",
      "recalling_firm": "Intuitive Surgical, Inc.",
      "address_1": "1266 Kifer Rd Bldg 100",
      "address_2": "N/A",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution Only",
      "recall_number": "Z-1424-2013",
      "product_description": "User Manual  addendum, TORS for da Vinci Surgical System IS 1200, IS 2000 and IS 3000.    Product Usage:  The user manual for Transoral Surgery (TORS) provided information to update and replace the Indications for Use and Representative uses section and add the section Warnings for Transoral Otolaryngology Surgery.",
      "product_quantity": "1,374",
      "reason_for_recall": "Change to User Manual to remove one indication for use and amend warnings to emphasize restrictions for use.",
      "recall_initiation_date": "20130124",
      "center_classification_date": "20130529",
      "termination_date": "20130530",
      "report_date": "20130605",
      "code_info": "Model number 552002-01"
    }
  ]
}