{
  "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": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73333",
      "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": "US: Nationwide  OUS: Canada, Afghanistan  Albania  Algeria  Andorra  Argentina  Australia  Austria  Azerbaijan  Bahamas  Bangladesh  Belarus  Belgium  Bolivia  Bosnia and Herzegovina  Botswana  Brazil  Burkina Faso  Chile  China  Colombia  Columbia  Congo, Democratic  Costa Rica  Croatia  Cyprus  Czech Republic  Denmark  Dominican Republic  Ecuador  Egypt  Estonia  Ethiopia  Finland  France  Georgia  Germany  Ghana  Greece  Guadeloupe  Hong Kong  Hungary  Iceland  India  Indonesia  Iran  Iraq  Ireland  Israel  Italy  Japan  Jersey  Jordan  Kazakhstan  Kenya  Korea, Republic of  Kuwait  Kyrgyzstan  Latvia  Lebanon  Libya  Lithuania  Luxembourg  Malaysia  Malta  Martinique  Mauritius  Mexico  Monaco  Mongolia  Morocco  Mozambique  Nepal  Netherlands  New Caledonia  New Zealand  Norway  Oman  Pakistan  Palestinian territory, occupied  Panama  Papua New Guinea  Peru  Philippines  Poland  Portugal  Puerto Rico  Romania  Russian Federation  Rwanda  Saudi Arabia  Serbia  Singapore  Slovakia  Slovenia  South Africa  Spain  Sri Lanka  Sudan  Sweden  Switzerland  Syrian Arab Republic  Taiwan  Tanzania  Thailand  Tunisia  Turkey  Uganda  Ukraine  United Arab Emirates  United Kingdom  Venezuela  Viet Nam  Yemen  Zimbabwe",
      "recall_number": "Z-1024-2016",
      "product_description": "SENSE Body Coil 1.5T with identification;  used in the ACS NT, Intera 1.5T and Achieva 1.5T MR system",
      "product_quantity": "5672",
      "reason_for_recall": "Wrong positioning of the coil cables can create unintended resonances via the patient or elevated coil cable temperature due to coupling to the QBC. The combined use of the Sense coil, high SAR level scanning and placement of the cables contrary to instructions for use can lead to patient burns.",
      "recall_initiation_date": "20150706",
      "center_classification_date": "20160226",
      "termination_date": "20170829",
      "report_date": "20160309",
      "code_info": "4522 131 5575x  4522 132 1985x  4522 132 7619x  4598 000 5187x  4598 000 5189x  4598 003 59051"
    }
  ]
}