{
  "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": "2026-04-22",
    "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": "70891",
      "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": "Worldwide Distribution - US including CA, FL, IL, IN,  MD, MI, MN, MO, NC, NY, OH, OR, PA, PR,  TX, VA,  WI  Foreign: Canada",
      "recall_number": "Z-1611-2015",
      "product_description": "FujiMedical Synapse Cardiovascular I ProSolv CardioVascular.     A picture Archiving and Communication System  Software versions:  Synapse Cardiovascular v4.0.8  Synapse Cardiovascular v4.0.8 SR1",
      "product_quantity": "30 units",
      "reason_for_recall": "Measurement values in the EMR may not accurately reflect the actual measurement value on the Synapse Cardiovascular 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": ""
    }
  ]
}