{
  "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": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79532",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Device is software only.  No products are distributed to wholesale dealers, distributers or retailers",
      "recall_number": "Z-1303-2018",
      "product_description": "Syngo.via.  Medical Device Software. Picture archiving and communications system.",
      "product_quantity": "236 units",
      "reason_for_recall": "A software functionality in the report sections  Findings Information  and  Summary of Measured Findings  is not performing properly. The system will use the original values instead of displaying and saving corrected/modified values. Outdated information could be sent to the referring physician when creating the formal report in the reporting system.",
      "recall_initiation_date": "20180108",
      "center_classification_date": "20180403",
      "termination_date": "20200422",
      "report_date": "20180411",
      "code_info": "Model Number 10496180"
    }
  ]
}