{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94090",
      "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": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide, including Puerto Rico and the countries of  Australia, Belgium, Brazil, Canada, Colombia, Ecuador, France, Germany, India, Italy, Mexico, Namibia, Netherlands, Portugal, Qatar, Spain, Thailand, Turkey, UAE, United Kingdom.",
      "recall_number": "Z-1269-2024",
      "product_description": "Synapse PACS - Version 7.1.000US",
      "product_quantity": "3 Units (3 US)",
      "reason_for_recall": "Measurements on a Secondary Capture 2D image, that does not have pixel spacing in the DICOM header, when combined with a Breast Tomo Series results in incorrect measurements.",
      "recall_initiation_date": "20240110",
      "center_classification_date": "20240307",
      "report_date": "20240313",
      "code_info": "Software Version: 7.1.000US, UDI: (01)854904006008(10)0701000US",
      "more_code_info": ""
    }
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}