{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "Sunnyvale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68593",
      "recalling_firm": "Intuitive Surgical, Inc.",
      "address_1": "1266 Kifer Rd Bldg 100",
      "address_2": "",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Worldwide Distribution.",
      "recall_number": "Z-1994-2014",
      "product_description": "Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system.    Intuitive Surgical Inc.  Sunnyvale, CA 94086",
      "product_quantity": "2606",
      "reason_for_recall": "Patient Side Cart battery boxes may overheat in rare charging conditions, causing battery bulging.",
      "recall_initiation_date": "20120427",
      "center_classification_date": "20140704",
      "termination_date": "20140707",
      "report_date": "20140716",
      "code_info": "Material number 371268-02 - al lots.",
      "more_code_info": ""
    }
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}