{
  "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": "63709",
      "recalling_firm": "Philips Healthcare Inc.",
      "address_1": "3000 Minuteman Road",
      "address_2": "N/A",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Canada.",
      "recall_number": "Z-0495-2013",
      "product_description": "Philips IntelliVue Information Center/Client and Philips IntelliVue Information Center iX     The intended use of the Information Center Software is to display physiologic waves, parameters, and trends, format data for strip chart 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 of the Information Center Software is to provide primary annunciation of alarms and configuration and control access for networked telemetry monitors.",
      "product_quantity": "3165",
      "reason_for_recall": "Internal audio cable may have diminished retention force due to damaged contacts, which could lead to intermittent or loss of audible alarms.",
      "recall_initiation_date": "20121109",
      "center_classification_date": "20121210",
      "report_date": "20121219",
      "code_info": "PIIC  865435 M3140 Information Center Low Acuity  865436 M3150 Information Center Local DB  865417 M3145 Information Center Small NW DB  865418 M3155 Information  Center NW DB  865415 M3151 Information Center Client  865421 \u0013 M3170 Patient Link  865416 \u0013 M3177 Trend Display  865422 \u0013 M3140 Upgrade  865423 \u0013 M3150 Upgrade  865426 \u0013 M3145 Upgrade  865427 \u0013 M3155 Upgrade  865424 \u0013 M3151 Upgrade  865266 - M3140 Information Center Low Acuity  865267 \u0013 M3150 Information Center Local DB  865269 \u0013 M3145 Information Center Small NW DB  865268 \u0013 M3155 Information Center NW DB  865270 \u0013 M3151 Information Center Client  865274 \u0013 M3170 Patient Link  865271 \u0013 M3177 Trend Display  865277 \u0013 M3140 Upgrade  865278 \u0013 M3150 Upgrade  865281 \u0013 M3145 Upgrade  865282 \u0013 M3155 Upgrade  865279 \u0013 M3151 Upgrade    PIIC iX  866023 \u0013 IntelliVue Info Center iX  866117 \u0013 PIIC Classic Upgrade  866027 \u0013 PIIC iX HW Upgrade"
    }
  ]
}