{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "Philips Intellivue and Avalon Fetal Monitors in time-synchronized automatic/sequence mode, the NBP automatic measurement series is stopped",
      "address_2": "",
      "product_quantity": "7587 units",
      "code_info": "software revisions J.21.03,  J.21.19",
      "center_classification_date": "20141021",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  AUSTRALIA AUSTRIA BAHRAIN BELGIUM CHINA COLOMBIA CZECH REPUBLIC DENMARK FINLAND FRANCE GERMANY HONG KONG INDIA IRELAND ISRAEL ITALY JAPAN KAZAKHSTAN NETHERLANDS NEW ZEALAND NICARAGUA NIGERIA NORWAY OMAN POLAND ROMANIA RUSSIA SINGAPORE SLOVENIA SOUTH AFRICA SOUTH KOREA SPAIN SWEDEN SWITZERLAND TAIWAN THAILAND TURKEY UKRAINE and UNITED KINGDOM.",
      "state": "MA",
      "product_description": "Philips IntelliVue Monitors with software revisions J.21.03,  J.21.19.     Model\t\tProduct  MP5\t\tM8105A;  MP5SC\t\tM8105AS;  MP5T \t\tM8105AT;  MP5 Upgrade\tM8105AU ;  MP5SC Upgrade\t866327    The monitors are intended to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates.",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems, Inc.",
      "recall_number": "Z-0104-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69348",
      "termination_date": "20170131",
      "more_code_info": "",
      "recall_initiation_date": "20141003",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}