{
  "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": "Littleton",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76090",
      "recalling_firm": "Mevion Medical Systems, Inc.",
      "address_1": "300 Foster Street",
      "address_2": "N/A",
      "postal_code": "01460-2017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide in the states of OK,  NJ",
      "recall_number": "Z-1122-2017",
      "product_description": "MEVION S250-Proton Radiation Therapy    Product Usage:  Proton Radiation Therapy",
      "product_quantity": "2 units",
      "reason_for_recall": "An error can occur causing Delta corrections to be lost when one setup field is closed and another is opened",
      "recall_initiation_date": "20161216",
      "center_classification_date": "20170202",
      "termination_date": "20170413",
      "report_date": "20170208",
      "code_info": "S250-0002 and S250-0003",
      "more_code_info": ""
    }
  ]
}