{
  "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": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99865",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "",
      "postal_code": "02141-2289",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "",
      "distribution_pattern": "U.S. and U.S. Territories.",
      "recall_number": "Z-3155-2026",
      "product_description": "Philips Medical Systems  Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333",
      "product_quantity": "62",
      "reason_for_recall": "The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.",
      "recall_initiation_date": "20260818",
      "center_classification_date": "20260929",
      "report_date": "20261007",
      "code_info": "UDI: (01)00884838101111",
      "more_code_info": ""
    }
  ]
}