{
  "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": "Veenendaal",
      "state": "N/A",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84371",
      "recalling_firm": "Nucletron BV",
      "address_1": "Waardgelder 1",
      "address_2": "POBox 930",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in United States and worldwide",
      "recall_number": "Z-0772-2020",
      "product_description": "There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy afterloader system. Due to an obstruction during the check cable out drive, the internal guiding tube became displaced and the check cable became damaged. This issue could cause treatment interruption or in a very unlikely scenario, incorrect source positioning and radiation treatment errors.",
      "product_quantity": "383",
      "reason_for_recall": "A component failure may lead to treatment interruption or incorrect source positioning.",
      "recall_initiation_date": "20191118",
      "center_classification_date": "20200102",
      "termination_date": "20230328",
      "report_date": "20200108",
      "code_info": "REF 136149A02; UDI: (01)08717213051126 (11)171127 (21)FT00340 (240)136149"
    }
  ]
}