{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Saint Charles",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88451",
      "recalling_firm": "Elekta Inc",
      "address_1": "1450 Beale St Ste 205",
      "address_2": "N/A",
      "postal_code": "63303",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in US - IA, NJ, NY, TN, PA, TX, and WI  OUS distribution in Australia, Bahrain, Belgium, Canada, China, Denmark, France, Germany, Hong Kong, Italy, Japan, Korea, Netherlands, Spain, Sweden, Switzerland, Thailand, Turkey and United Kingdom",
      "recall_number": "Z-2406-2021",
      "product_description": "Monaco RTP System, Software Builds 5.40.00, 5.40.01, 5.40.02, and 5.51.10",
      "product_quantity": "N/A",
      "reason_for_recall": "If a couch is removed while a plan is loaded, and then added back to the Studyset when the plan is unloaded, it is possible to calculate dose with the couch unassigned to the beams.",
      "recall_initiation_date": "20210726",
      "center_classification_date": "20210902",
      "report_date": "20210908",
      "code_info": "Software Builds: 5.40.00, 5.40.01, 5.40.02, 5.51.10  UDI: (01)00858164002190(10) 5.40.00 (01)00858164002190(10) 5.40.01 (01)00858164002190(10) 5.40.02 (01)00858164002268(10) 5.51.10"
    }
  ]
}