{
  "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": "72210",
      "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": "Letter",
      "distribution_pattern": "US nationwide distribution including FL, NJ, OK, and MO.",
      "recall_number": "Z-0767-2016",
      "product_description": "MEVION S250 Radiation therapy system",
      "product_quantity": "4",
      "reason_for_recall": "The treatment table positioning belt can slip gear positions, resulting in deviation of patient setup and treatment positions from the time of slippage until the discovery of slippage and the halting of treatment.",
      "recall_initiation_date": "20151118",
      "center_classification_date": "20160208",
      "termination_date": "20170403",
      "report_date": "20160217",
      "code_info": "Manufacturing Lot or Serial Number: S250-0004",
      "more_code_info": ""
    }
  ]
}