{
  "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,
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      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90751",
      "recalling_firm": "FUJIFILM Healthcare Americas Corporation",
      "address_1": "81 Hartwell Ave Ste 300",
      "address_2": "",
      "postal_code": "02421-3160",
      "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",
      "recall_number": "Z-1748-2022",
      "product_description": "SCENARIA View: Software Version V1.08, V1.09B, V1.09C, V1.09D, V1.0B, V1.0C",
      "product_quantity": "46 units",
      "reason_for_recall": "Error 00003050 or 00003052  may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation",
      "recall_initiation_date": "20220712",
      "center_classification_date": "20220915",
      "report_date": "20220921",
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