{
  "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": "Terminated",
      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87938",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "81 Hartwell Ave Ste 300",
      "address_2": "",
      "postal_code": "02421-3160",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and the countries of Canada, Bermuda, Israel, Hadassah Medical Center.",
      "recall_number": "Z-1775-2021",
      "product_description": "Synapse Cardiovascular (Synapse CV).   Software Versions: 6.0 to 6.2.1  The Synapse Cardiovascular image is a management and reporting system",
      "product_quantity": "44 US and 4 OUS",
      "reason_for_recall": "Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that a previously assigned internal patient database ID can be reused for a new patient.  It was discovered that this value does not increase when a patient merge activity is executed in a specific sequence",
      "recall_initiation_date": "20210430",
      "center_classification_date": "20210602",
      "termination_date": "20240729",
      "report_date": "20210609",
      "code_info": "Software Versions: 6.0 to 6.2.1",
      "more_code_info": ""
    }
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}