{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99730",
      "recalling_firm": "Volcano Corp",
      "address_1": "3721 Valley Centre Dr Ste 500",
      "address_2": "",
      "postal_code": "92130-3328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of MA, MN, TX, AL, GA, CA and the countries of Belgium, Denmark, Germany, Netherlands, Poland, Spain, Sweden, United Kingdom.",
      "recall_number": "Z-3276-2026",
      "product_description": "Philips IntraSight Plus  REF: 797423 and 797417  100-120v-220-240v,50/60hZ, 1000 VA",
      "product_quantity": "19 systems",
      "reason_for_recall": "Software system  may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.",
      "recall_initiation_date": "20260806",
      "center_classification_date": "20260925",
      "report_date": "20261007",
      "code_info": "UDI:  REF: 797423:(01)00845225012946/REF:797417: (01)00845225012939 all Philips IntraSight Plus Systems with Software Version 6.0.4",
      "more_code_info": ""
    }
  ]
}