{
  "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": "2026-04-15",
    "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": "98675",
      "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 - US Nationwide distribution.",
      "recall_number": "Z-1653-2026",
      "product_description": "ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.",
      "product_quantity": "U.S. 758, OUS 2077",
      "reason_for_recall": "During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient.  Despite the reported dose showing significantly higher, the actual applied x-ray dose levels are in accordance with the system  settings and imaging conditions, as well as the applicable regulatory requirements.",
      "recall_initiation_date": "20260310",
      "center_classification_date": "20260407",
      "report_date": "20260415",
      "code_info": "ARTIS pheno UDI: 4056869046877. ARTIS icono biplane UDI: 4056869063317. ARTIS icono ceiling UDI: 4056869295923. ARTIS icono floor UDI: 4056869149325.",
      "more_code_info": ""
    }
  ]
}