{
  "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": "2026-06-24",
    "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": "98992",
      "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": "US and Worldwide",
      "recall_number": "Z-2205-2026",
      "product_description": "ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system",
      "product_quantity": "",
      "reason_for_recall": "During patient examinations, the system may sporadically display a  0  x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing  0,   an actual x-ray dose is applied to the patient.",
      "recall_initiation_date": "20260309",
      "center_classification_date": "20260604",
      "report_date": "20260610",
      "code_info": "UDI: 4056869046877",
      "more_code_info": ""
    }
  ]
}