{
  "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): 5097  5426  5519  5507  5255  5059  5379  5257  5316  5144  5002  5300  5440  5482  5014  5492  5019  5423  5256  5293  5382  5319  5420  5030  5477  5488  5193  5085  5347  5287  5195  5481  5370  5474  5360  5352  5106  5135  5495  5313  5413  5245  5142  5378  5411  5214  5151  5053  5222  5201  5381  5246  5306  5429  5441  5324  5273  5048  5124  5211  5453  5277  5533  5239  5248  5349  5414  5311  5513  5204  5215  5434  5577  5296  5259  5271  5512  5373  5542  5290  5091  5446  5266  5406  5551  5090  5455  5123  5261  5323  5390  5254  5353  5502  5241  5514  5238  5035  5105  5333  5454  5226  5334  5328  5417  5298  5451  5288  5200  5077  5250  5342  5309  5172  5432  5081  5199  5458  5573  5568  5268  5110  5472  5052  5009  5461  5022  5297  5263  5158  5078  5230  5558  5428  5303  5376  5515  5520  5269  5394  5253  5282  5042  5155  5084  5047  5530  5501  5383  5497  5016  5329  5162  5143  5491  5470  5566  5071  5079  5258  5125  5283  5129  5475  5574  5149  5018  5421  5473  5227  5330  5264  5132  5141  5327  5265  5351  5121  5216  5236  5180  5487  5478  5116  5160  5345  5301  5522  5083  5391  5021  5552  5314  5363  5024",
      "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": "ACS-NT, Model 78108    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-1439-2018",
      "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"
    }
  ]
}