{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Foster City",
      "address_1": "4100 E 3rd Ave Ste 101",
      "reason_for_recall": "A problem was detected in the Philips IntelliSpace PAC 4.4 software where  if patient information is changed in the DICOM header and the study is exported before the image is updated in the PACS, the unchanged data may export causing the potential for diagnosis on incomplete data.",
      "address_2": "",
      "product_quantity": "109 units",
      "code_info": "IntelliSpace 4.4",
      "center_classification_date": "20140815",
      "distribution_pattern": "US and  Australia, Belgium, Canada, Egypt, France, Germany, Netherlands, Oman, Saudi Arabia, Spain, Switzerland, United Arab Emirates, United Kingdom.",
      "state": "CA",
      "product_description": "Philips IntelliSpace PACS 4.4 image management systems performs digital image processing, measurement and communication and storage.",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare Informatics, Inc.",
      "recall_number": "Z-2252-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68979",
      "termination_date": "20160211",
      "more_code_info": "",
      "recall_initiation_date": "20140724",
      "postal_code": "94404-4819",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}