{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90246",
      "recalling_firm": "Canon Medical System, USA, INC.",
      "address_1": "2441 Michelle Dr",
      "address_2": "",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, CO, FL, NY, and WY  O.U.S.: None",
      "recall_number": "Z-1289-2022",
      "product_description": "System: Alphenix 4D CT in combination with CAS-930A (C arm Support)    Model Number:  INFX-8000C/BF,  INFX-8000C/BH,  INFX-8000C/SW",
      "product_quantity": "6 systems",
      "reason_for_recall": "CT operation may be restricted by an interlock which is a result of an system error and the CT system may stop operating properly after an attempt to cancel the error message has been initiated.",
      "recall_initiation_date": "20220503",
      "center_classification_date": "20220624",
      "report_date": "20220706",
      "code_info": "UDI-DI Code: 04987670100192  Model Number: INFX-8000C/BF Serial Number/SID: BFA18Y7001 / 30038795  Model Number: INFX-8000C/BH Serial Number / SID: BHB2132002 / 30039730 BHB2132003/ 30039787 BHA1992001 / 30043325 BHC21X2004 / Not Provided  Model Number: INFX-8000C/SW Serial Numbers/SID: SWB2162001 / 30052648",
      "more_code_info": ""
    }
  ]
}