{
  "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": "2026-04-01",
    "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": "85799",
      "recalling_firm": "Philips North  America, LLC",
      "address_1": "3000 Minuteman Rd",
      "address_2": "",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  Angola  Angola  Argentina  Australia  Austria  Bahrain  Belarus  Belgium  Bolivia  Brazil  Bulgaria  Canada  Chile  China  Colombia  Costa Rica  Croatia  Cyprus  Czech Republic  Denmark  Egypt  Estonia  Finland  France  French Guiana  Germany  Ghana  Gibraltar  Greece  Greenland  Guadeloupe  Guatemala  Hong Kong  Hungary  Iceland  India  Indonesia  Iran  Ireland  Israel  Italy  Japan  Jordan  Kazakhstan  Kenya  Korea, Republic of  Kuwait  Latvia  Lebanon  Lithuania  Luxembourg  Malaysia  Martinique  Mexico  Morocco  Mozambique  Namibia  Netherlands  New Caledonia  New Zealand  Nicaragua  Norway  Oman  Palestine, State of  Paraguay  Peru  Philippines  Poland  Portugal  Qatar  R¿union  Russian Federation  Saint Pierre and Miquelon  Saudi Arabia  Singapore  Slovakia  Slovenia  South Africa  Spain  Sri Lanka  Sweden  Switzerland  Syrian Arab Republic  Taiwan  Tanzania  Thailand  Turkey  Ukraine  United Arab Emirates  United Kingdom",
      "recall_number": "Z-2531-2020",
      "product_description": "Philips M3015A  Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MMX Multi-Measurement Module (Model No. 867036)",
      "product_quantity": "46,597 Units WW",
      "reason_for_recall": "Affected M3015A extensions are incompatible with the lntelliVue X3 Patient Monitor (Model No. 867030) and lntelliVue MMX multi-measurement server (Model No. 867036).If they are connected to a host monitor, communication with the X3 or MMX could be disrupted, resulting in a loss of monitoring on the host monitor.",
      "recall_initiation_date": "20200608",
      "center_classification_date": "20200707",
      "termination_date": "20230109",
      "report_date": "20200715",
      "code_info": "Units with this hardware version can be identified by the following serial number prefix: SN prefix: DE435xxxxx (first five digits)",
      "more_code_info": ""
    }
  ]
}