{
  "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": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "4615 Southwest Fwy Ste 330",
      "reason_for_recall": "Mobius3D version 1.5.0 contained a defect in software code which affects users who perform beam customization, and may lead to a discrepancy in dose calculation between this version of Mobius3D (1.5.0) and the prior version (1.4.2), where none should have been expected.",
      "address_2": "",
      "product_quantity": "270",
      "code_info": "Version 1.5.0 and 1.5.2 of the Mobius3D software is affected.",
      "center_classification_date": "20170516",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Sweden, Canada, Netherlands, Denmark, Spain, Switzerland, Australia, Austria, Israel, United Kingdom, France",
      "state": "TX",
      "product_description": "Mobius3D    Product Usage:  Mobius3D software is used for quality assurance and treatment plan verification in radiation therapy. It calculates radiation dose three-dimensionally in a representation of a patient or a phantom. The calculation is based on read-in treatment plans that are initially calculated by a treatment planning system, and may additionally be based on external measurements of radiation fields from other sources such as linac delivery log data. Mobius3D is not a treatment planning system. It is only to be used by trained radiation oncology personnel as a quality assurance tool.",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mobius Medical Systems, LP",
      "recall_number": "Z-2100-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77177",
      "termination_date": "20170710",
      "more_code_info": "",
      "recall_initiation_date": "20150223",
      "postal_code": "77027-7106",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}