{
  "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": "92664",
      "recalling_firm": "Canon Medical System, USA, INC.",
      "address_1": "2441 Michelle Dr",
      "address_2": "N/A",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution: NY, CO, IL, CA, MD, MN, WA",
      "recall_number": "Z-2392-2023",
      "product_description": "INFX-8000C XGCP-930AA TABLE SIDE CONSOLE,  INFX-8000C XGCP-930BA TABLE SIDE CONSOLE",
      "product_quantity": "12",
      "reason_for_recall": "The C-arm, used to set the position and angle of the x-ray exposure field, may not function due to the tableside console PWB, which needs replacement. There may be a delay in the procedure, but procedures can continue using the operators console, the switches on the back of the column, switches on the side of the flat panel detector, and the emergency stop will continue to function normally.",
      "recall_initiation_date": "20230622",
      "center_classification_date": "20230810",
      "report_date": "20230816",
      "code_info": "UDI-DI: 04987670100192. INFX-8000C, Serial Numbers: BHA1992001, BHB2132003, SWC2242002, AFB1832003, SUC2262008, SUC2292010, BFB1972004, SUB2172002, SWC2262003"
    }
  ]
}