{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "72537",
      "product_res_number": "Z-0014-2009",
      "event_date_initiated": "2008-06-20",
      "event_date_posted": "2008-10-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-04-05",
      "res_event_number": "49022",
      "product_code": "LHN",
      "k_numbers": [
        "K981112"
      ],
      "product_description": "Mobetron Model 1000, mobile electron linear accelerator, a device system which delivers radiation to an intraoperative site.",
      "code_info": "all units",
      "firm_fei_number": "3001874253",
      "recalling_firm": "Intraop Medical Corporation",
      "address_1": "570 Del Rey Ave",
      "city": "Sunnyvale",
      "state": "CA",
      "postal_code": "94085-3528",
      "additional_info_contact": "408-636-1020 Ext. 109",
      "reason_for_recall": "Docking screw/nut  failure, which may result in a treatment head dropping, potentially impacting the patient.",
      "root_cause_description": "Component design/selection",
      "action": "Recall initiated on 06/20/2008, advising users via Advisory Notice that a safety upgrade would be available.  Two options are given to either self inspect the product or schedule an Intraop Authorized Field Service Engineer to visit their facility to perform the inspection.  The letter notes that if no nut failure was evident, the machine could still be used.  The firm continues to send retrofit kits.",
      "product_quantity": "24 units",
      "distribution_pattern": "Worldwide Distribution",
      "openfda": {
        "k_number": [
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        "device_name": "System, Radiation Therapy, Charged-Particle, Medical",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.5050",
        "device_class": "2"
      }
    }
  ]
}