{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97135",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "",
      "postal_code": "19355-1418",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "",
      "distribution_pattern": "Worldwide.",
      "recall_number": "Z-2020-2025",
      "product_description": "interventional fluoroscopic x-ray system",
      "product_quantity": "",
      "reason_for_recall": "In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.",
      "recall_initiation_date": "20250515",
      "center_classification_date": "20250627",
      "report_date": "20250709",
      "code_info": "4056869063317",
      "more_code_info": ""
    }
  ]
}