{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Stamford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70890",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "419 West Ave",
      "address_2": "N/A",
      "postal_code": "06902-6343",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including PR and the states of IL, IN, FL, GA, MD, MI, MO, MS, NC, NY, OR, and PA, PR  and the country of Canada.",
      "recall_number": "Z-1612-2015",
      "product_description": "Fujifilm Synapse Cardiovascular I ProSolv CardioVascular  Synapse Cardiovascular v4.0.8  Synapse Cardiovascular v4.0.8 SR1     Intended Use:  Picture Archiving and Communication System  Computer, Diagnostic, Programmable",
      "product_quantity": "16 units",
      "reason_for_recall": "Under certain circumstances the patient  Demographics in a report exported into the EMR may not match the demographics shown in the corresponding Synapse CV clinical report.",
      "recall_initiation_date": "20150204",
      "center_classification_date": "20150514",
      "termination_date": "20180920",
      "report_date": "20150520",
      "code_info": "Software Versions:  Synapse Cardiovascular v4.0.8  Synapse Cardiovascular v4.0.8 SR1",
      "more_code_info": ""
    }
  ]
}