{
  "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): 4170  4113  4082  4176  4147  4319  4397  4285  4308  4408  4241  4064  4328  4312  4294  4296  4009  4274  4258  4297  4246  4200  4041  4207  4327  4318  4089  4102  4222  4025  4321  4177  4015  4088  4106  4260  4183  4272  4416  4365  4047  4411  4254  4301  4261  4307  4267  4386  4033  4099  4251  4339  4374  4162  4322  4320  4069  4006  4273  4418  4131  4194  4201  4152  4146  4095  4391",
      "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": "T10-NT, Model 78107    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-1440-2018",
      "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"
    }
  ]
}