{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "1266 Kifer Rd Bldg 100",
      "reason_for_recall": "B. Braun 2 gang 4-way stopcocks in the Fluorescence  Imaging Procedure Kit may experience damage to the sterile packaging during shipping. The damage can  result in tears to the packaging and has the potential to cause a breach in sterility of the supplied stopcocks.",
      "address_2": "",
      "product_quantity": "1200 kits",
      "code_info": "Product number: 950156-01:  Lot numbers:  NQ141201  NQ141502  NQ142201  NQ142901  NQ143201  NQ143301.    Product number 950156-02:  Lot numbers:  NQ143501  NQ143502  NQ143601  NQ143602  NQ143803  NQ143901  NQ143902.    Product number 950156-03:  Lot numbers :  NQ144001 NQ150501   NQ143902 NQ150601   NQ143901 NQ150602   NQ143803 NQ150703   NQ143601 NQ150701   NQ143602 NQ150702   NQ144502 NQ150801   NQ144801 NQ150901   NQ145202 NQ150802   NQ144901 NQ151001   NQ145301 NQ151002   NQ145201 NQ151101   NQ150301 NQ150501   NQ144001.",
      "center_classification_date": "20150917",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "CA",
      "product_description": "Fluorescence Imaging Procedure Kits used with the da Vinci Si and Xi Surgical Systems;  Model numbers: 950156-01, 950156-02, 950156-03.    Product Usage:  General and plastic surgery: The da Vinci Firefly Imaging system is intended to provide real-time endoscopic visible and near-infrared fluorescence imaging.",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Intuitive Surgical, Inc.",
      "recall_number": "Z-2782-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72158",
      "termination_date": "20151102",
      "more_code_info": "",
      "recall_initiation_date": "20150909",
      "postal_code": "94086-5304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}