{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90737",
      "recalling_firm": "Canon Medical System, USA, INC.",
      "address_1": "2441 Michelle Dr",
      "address_2": "",
      "postal_code": "92780-7047",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1666-2022",
      "product_description": "INFX-8000V.  For radiographic and fluoroscopic studies and intervention.",
      "product_quantity": "16 systems",
      "reason_for_recall": "The fluoroscopic dose rate might exceed the conforming value during biplane fluoroscopy.",
      "recall_initiation_date": "20220131",
      "center_classification_date": "20220901",
      "report_date": "20220907",
      "code_info": "Model:  Alphenix i with software version 8.0, 9.0 or 9.2 and the TFP 1200C FPD.",
      "more_code_info": ""
    }
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}