{
  "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": "2026-03-18",
    "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": "92238",
      "recalling_firm": "PHILIPS HEADQUARTERS CAMBRIDGE",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AR, CA, OK, TX Foreign: Country Argentina Australia Austria China Colombia Czech Republic Dominican Rep France Germany Guadeloupe Hong Kong India Japan Kuwait Latvia Lithuania Netherlands Norway Portugal Romania Spain Switzerland Taiwan Thailand United Kingdom Vietnam",
      "recall_number": "Z-1625-2023",
      "product_description": "Incisive CT Plus -Whole-body computed tomography (CT) X-Ray System   Model Number: 728149  (OUS)",
      "product_quantity": "5 units",
      "reason_for_recall": "Potential for Incorrect Image Orientation resulting images may be flipped or reversed result in misdiagnosis, incorrect treatment of a condition, or additional radiation exposure if a rescan is required",
      "recall_initiation_date": "20230412",
      "center_classification_date": "20230523",
      "report_date": "20230531",
      "code_info": "UDI-DI: (01)00884838103474(21)  Serial Number: 530537 554032 554060 554065 554078"
    }
  ]
}