{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86532",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "81 Hartwell Ave Ste 300",
      "address_2": "N/A",
      "postal_code": "02421-3160",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Software was distributed to medical facilities nationwide throughout the U.S.",
      "recall_number": "Z-0878-2021",
      "product_description": "Synapse PACS Software Versions 5.1 and higher",
      "product_quantity": "235",
      "reason_for_recall": "There is a potential for the wrong patient information may be displayed in the viewer or PowerJacket. Additionally, the incorrect max standard uptake values (SUV) for PET ad CT studies may be returned for Siemens Modality.",
      "recall_initiation_date": "20200911",
      "center_classification_date": "20210116",
      "report_date": "20210127",
      "code_info": "Software Versions 5.1, 5.2, 5.3, 5.4, 5.5, and 5.7.",
      "more_code_info": ""
    }
  ]
}