{
  "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": "2026-09-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99784",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US and US Territories.",
      "recall_number": "Z-3042-2026",
      "product_description": "Philips Ingenuity CT  Product Codes: Ingenuity CT Upgrades 728327,   Ingenuity CT China 728324,  Ingenuity Core 128 Elite Brazil 728325.   Software 4.4.10.x",
      "product_quantity": "N/A",
      "reason_for_recall": "Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.",
      "recall_initiation_date": "20260807",
      "center_classification_date": "20260901",
      "report_date": "20260909",
      "code_info": "UDI:  Ingenuity CT Upgrades (01)00884838098701, Ingenuity CT China (01)00884838059863, Ingenuity Core 128 Elite Brazil: N/A",
      "more_code_info": ""
    }
  ]
}