{
  "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": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89260",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0515-2022",
      "product_description": "Artis pheno  with software VE20C- diagnostic imaging angiography system  Model:  10849000",
      "product_quantity": "12 units",
      "reason_for_recall": "Four potential software issues with Artis pheno and Artis icono systems with software VE20C: 1.\tUpdated calibration data not saved with measurement after scene+/-; 2.\tNo x-ray possible, system shutdown/restart might be required during intervention; 3. Corrupted Image during Roadmap;  4.\tUnintended shutdown of Imaging System with UPS (Uninterruptable Power Supply) option",
      "recall_initiation_date": "20211012",
      "center_classification_date": "20220121",
      "termination_date": "20240411",
      "report_date": "20220202",
      "code_info": "Serial Numbers: 164719 164712 164722 164723 164728 164711 164718 164703 164721 164726 164724 164725  UDI: 04056869046877",
      "more_code_info": ""
    }
  ]
}