{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "95226",
      "product_res_number": "Z-0414-2011",
      "event_date_initiated": "2010-10-19",
      "event_date_posted": "2010-11-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2017-08-01",
      "res_event_number": "57039",
      "product_code": "DXJ",
      "k_numbers": [
        "K992636"
      ],
      "product_description": "Philips IntelliVue Clinical Information Portfolio (ICIP), Clinical Management System\nSoftware Version D.00 through D.03.",
      "code_info": "Philips IntelliVue Clinical Information Portfolio Release D.XX, where XX is 00, 01, 02 or 03.",
      "firm_fei_number": "1218950",
      "recalling_firm": "Philips Healthcare Inc.",
      "address_1": "3000 Minuteman Road",
      "city": "Andover",
      "state": "MA",
      "postal_code": "01810",
      "additional_info_contact": "978-687-1501",
      "reason_for_recall": "Software: Scheduling function of the Philips Intellivue Clinical Information Portfolio Releases D.00 through D.03.  Edits to a scheduled even frequency order may result in pending interventions not being generated after the first 24 hours.",
      "root_cause_description": "Software design",
      "action": "Philips Healthcare issued an Urgent Medical Device Correction letter dated October 15, 2010 to customers. \nCustomers are asked to follow the guidelines in the \"Action to be taken by Customer/User\" section of the Urgent Medical Device Correction Notice until they receive their software correction.  The correction will be in the form of a software upgrade and will be performed by Philips service personnel. Contact Philips Customer Care Center with questions or concerns about this correction at 1-800-722-9377",
      "product_quantity": "200 units",
      "distribution_pattern": "Worldwide Distribution: USA, including states of CA, DC, FL, IL, IN, KY, MA, MD, ME, NJ, NY, OK, RI, TX, VA, VT, and WV; and the countries of: AUSTRALIA, AUSTRIA, BELGIUM, CANADA, CHINA, CZECH REPUBLIC, DENMARK, FINLAND, FRANCE, GERMANY, HONG KONG, IRELAND, ITALY, KENYA, LATVIA, MALAYSIA, NETHERLANDS, NORWAY, SAUDI ARABIA, SINGAPORE, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, PROVINCE OF CHINA, THAILAND, UNITED ARAB EMIRATES, and the UNITED KINGDOM.",
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        "device_name": "Display, Cathode-Ray Tube, Medical",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2450",
        "device_class": "2"
      }
    }
  ]
}