{
  "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": "2026-08-05",
    "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": "99352",
      "recalling_firm": "PHILIPS MEDICAL SYSTEMS",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution including Puerto Rico",
      "recall_number": "Z-2652-2026",
      "product_description": "Ingenuity CT  CT5000 Ingenuity Plus  CT5000 Ingenuity Pro  CT5000 Ingenuity Premium  Ingenuity CT Upgrades  Ingenuity CT China  Ingenuity Core 128 Elite Brazil",
      "product_quantity": "182",
      "reason_for_recall": "The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving additional radiation.",
      "recall_initiation_date": "20260611",
      "center_classification_date": "20260727",
      "report_date": "20260805",
      "code_info": "FCO72800815, FCO72800816, 728321 DI (01)00884838059498 728323 DI (01)00884838059504 728326 DI (01)00884838059511 728327 DI (01)00884838098701 728324 DI (01)00884838059863 728325"
    }
  ]
}