{
  "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-2650-2026",
      "product_description": "Brilliance iCT   Brilliance iCT Upgrades  Brilliance iCT SP  Brilliance CT 64 Channel  CT6000  Brilliance 64 Upgrades",
      "product_quantity": "128",
      "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  728305 728306 DI (01)00884838059474 728307 DI (01)00884838104600 728311  728231 (01)00884838083325  728232"
    }
  ]
}