{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "Potential risk for helium gas inside the MR examination room during a magnet quench",
      "address_2": "",
      "product_quantity": "8,205 units in total",
      "code_info": "(Added 6/25/18): 7149  7210  7082  7212  7015  7174  7081  10327  7073  10332  7063  7040  7119  7095  7272  10104  7005  7213  7057  10326  7128  10339  7230  10329  7183  7098  10053  7080  7011  7178  7139  7126  10192  7217  7066  7171  7136  7038  7050",
      "center_classification_date": "20180418",
      "distribution_pattern": "Worldwide Distribution - US Nationwide; International - Albania, Algeria, Andorra, Argentina, Australia, Austria, Bahamas, Bahrain, Bangladesh, Barbados, Belarus, Belgium, Bolivia,   Bosnia and Herzegovina, Botswana, Brazil, Bulgaria, Burkina Faso, Chile,  China, Colombia, Congo (Democratic Republic of the), Costa Rica,   C¿te D'Ivoire, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic,  Ecuador, Egypt, El Salvador, Ethiopia, Finland, France, Gabon, Georgia, Germany, Ghana, Greece, Guadeloupe, Guatemala, Hong Kong, Hungary,  Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jersey, Jordan,  Kazakhstan, Kenya, Republic of Korea - South Korea, Kuwait, Kyrgyzstan,   Latvia, Lebanon, Lesotho, Libya, Libyan Arab Jamahiriya, Lithuania, Luxembourg, Macedonia, Malaysia, Malta, Mauritius, Mexico, Monaco, Mongolia,  Montenegro, Morocco, Myanmar, Nepal, Netherlands, New Caledonia,   New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Palestine, State of  Panama, Papua New Guinea, Peru, Philippines, Poland, Portugal, Qatar,   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, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Venezuela,  Viet Nam, Yemen & Zimbabwe.",
      "state": "MA",
      "product_description": "Intera 1.0T; 1) Stellar Model 781102, 2) Pular Model 781103     Product Usage:  Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Electronics North  America Corporation",
      "recall_number": "Z-1432-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79451",
      "termination_date": "20200410",
      "more_code_info": "",
      "recall_initiation_date": "20180316",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}