{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "85943",
      "product_res_number": "Z-0418-2010",
      "event_date_initiated": "2009-10-21",
      "event_date_posted": "2009-11-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2016-08-22",
      "res_event_number": "53593",
      "product_code": "DXJ",
      "k_numbers": [
        "K992636"
      ],
      "product_description": "IntelliVue Clinical Information Portfolio (ICIP) Critical Care Release D, Version D.02.\n\nIntended for use in data collection, storage, and management with independent bedside devices, and ancillary systems that are connected either directly or through networks. It is indicated for use by healthcare providers whenever there is a need for generation of a patient record and computation of drug dosage.",
      "code_info": "S/W Version D.02",
      "firm_fei_number": "1218950",
      "recalling_firm": "Philips Healthcare Inc.",
      "address_1": "3000 Minuteman Road",
      "city": "Andover",
      "state": "MA",
      "postal_code": "01810",
      "additional_info_contact": "SAME\n978-687-1501",
      "reason_for_recall": "A software defect exists in the ICIP Release 0.02 scheduling function for order management such that if a user edits either the Schedule Time or the Stop Time for an existing order, the corresponding intervention(s) for the order may not be created.",
      "root_cause_description": "Software design",
      "action": "Philips Medical Systems notified accounts by letter on October 21, 2009, of the release ICIP version D.03, which  contains a software correction .  A Philips representative will schedule the implementation of this upgrade.  Please contact the Philips Customer Care Center with questions or concerns about this correction at 1-800-722-9377.",
      "product_quantity": "53 units",
      "distribution_pattern": "MD, RI, WV,  and TX\nAustralia\nBelgium\nDenmark\nFrance\nItaly\nMalaysia\nSingapore\nSpain\nSwitzerland\nTaiwan\nUnited Arab Emirates\nUnited Kingdom\nand\nIreland",
      "openfda": {
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          "K810164",
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          "K945277",
          "K103473",
          "K901072",
          "K831783",
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        ],
        "device_name": "Display, Cathode-Ray Tube, Medical",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2450",
        "device_class": "2"
      }
    }
  ]
}