{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Littleton",
      "address_1": "300 Foster St",
      "reason_for_recall": "Treatment is allowed to continue (via partials) in situations where dDose1 interlock has tripped",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "DI: (01)00864366000124  Serial Number: S250i-0007",
      "center_classification_date": "20190109",
      "distribution_pattern": "DC",
      "state": "MA",
      "product_description": "MEVION S250i",
      "report_date": "20190116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mevion Medical Systems, Inc.",
      "recall_number": "Z-0705-2019",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "81751",
      "termination_date": "20200410",
      "more_code_info": "",
      "recall_initiation_date": "20181001",
      "postal_code": "01460-2017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}