{
  "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": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "1266 Kifer Rd Bldg 101",
      "reason_for_recall": "The firm has identified the potential for a silicone particle to be generated within the Suction Irrigator device. If generated, a particle may be introduced into the patient with irrigation.",
      "address_2": "",
      "product_quantity": "3108 units (518 boxes of 6 units)",
      "code_info": "Lots: T10180226 and onward; Part Numbers: 480299-04 (UDI 00886874114810)",
      "center_classification_date": "20191030",
      "distribution_pattern": "Worldwide distribution.  US nationwide, Australia, Italy, Switzerland, and United Kingdom.",
      "state": "CA",
      "product_description": "EndoWrist Suction Irrigator, Single Use Instrument.  Part Number: 480299-04.    An accessory to the EndoWrist Surgical System, used in endoscopic surgery.",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Intuitive Surgical, Inc.",
      "recall_number": "Z-0249-2020",
      "initial_firm_notification": "Other",
      "product_type": "Devices",
      "event_id": "81073",
      "more_code_info": "",
      "recall_initiation_date": "20180604",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}