{
  "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-2651-2026",
      "product_description": "IQon Spectral CT  IQon Spectral CT Upgrades",
      "product_quantity": "42",
      "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": "FCO72800812; FCO72800814  728331 728332, DI (01)00884838059542"
    }
  ]
}