{
  "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": "None",
      "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": "Multiva systems; 1) Magnets Multiva 16 Model 781487, 2) Magnets 8 Model 781488, 3) Magnet Achieva 1.5T, Model 781492, 4) Magnet HFO, Model 781495, 5) Magnet Multiva 16, Model 781496, 6) Magnet Multiva 8, Model 781497 & 7) Magnets Ingenia 1.5T CX, Model 781498       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-1441-2018",
      "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"
    }
  ]
}