{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77437",
      "recalling_firm": "Philips Electronics North  America Corporation",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide)  OUS:   CANADA  ARGENTINA  AUSTRALIA  AUSTRIA  BAHRAIN  BELGIUM  BRAZIL  CHILE  CHINA  COLOMBIA  CZECH REPUBLIC  FINLAND  FRANCE  GERMANY  GREECE  INDIA  INDONESIA  IRELAND  ITALY  JAPAN  KENYA  KOREA, REPUBLIC OF  NETHERLANDS  PHILIPPINES  POLAND  SPAIN  SWEDEN  SWITZERLAND  THAILAND  TURKEY  UNITED KINGDOM",
      "recall_number": "Z-2528-2017",
      "product_description": "M3150 Information Center Local Database; Models: 862249, 865001, 865003, 865004, 865007, 865009, 865011, 865012, 865091, 865092, 865093, 865094, 865095, 865096, 865098, 865099, 865102, 865104, 865105, 865125, 865127.  The intended use of the Information Center Software is to display physiologic waves, parameters and trends, formal data for strip recordings and printed reports and provide the secondary annunciation of alarms from other networked medical devices at a centralized location. The Information Center Software provides for the retrospective review of alarms, physiologic waves and parameters from its database. An additional intended use is to provide primary annunciation of alarms and configuration and control access for networked telemetry monitors",
      "product_quantity": "607 units",
      "reason_for_recall": "Potential for early component failure.",
      "recall_initiation_date": "20101217",
      "center_classification_date": "20170613",
      "termination_date": "20170801",
      "report_date": "20170621",
      "code_info": "This action affects certain customers who were shipped an affected Philips Intellivue Information Center unit between  June 9, 2008 and May 31, 2009.  Affected products have a PC serial number range between 2UA8300XYZ and 2UA84510QW.  However, only a subset of these products are affected."
    }
  ]
}