{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88691",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of NV, AR MN.",
      "recall_number": "Z-0142-2022",
      "product_description": "Canon PET-CT SCANNER,  Cartesion Prime, MODEL PCD-1000A",
      "product_quantity": "3  units",
      "reason_for_recall": "A software problem has been identified which could result in the diagnostic imaging system  not proceeding to the next actual scan even though automatic start of the next scan is specified. This could result in the diagnostic imaging system  failing resulting in rescanning and reinjection of contrast medium.",
      "recall_initiation_date": "20201111",
      "center_classification_date": "20211019",
      "termination_date": "20230630",
      "report_date": "20211027",
      "code_info": "Affected serial numbers: 3DA1982001, 3DA2072002, 3DA2072003"
    }
  ]
}