{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "In Artis systems with A100G generators, a component can be affected by aging which could result in the potential failure of a module in the high-voltage generator.",
      "address_2": "",
      "product_quantity": "264 distributed worldwide (112 in the U.S.)",
      "code_info": "Model # 10848280, 10848281, 10848282, 10848283, 10848353, 10848354, 10848355    Serial # 109033  117012  121061  109080  109074  121006  121013  121040  105007  111005  109016  121062  111002  121082  121011  121039  123008  109066  109067  109068  121053  121054  117001  117023  123003  123011  109084  121014  121051  109011  121004  117021  121018  121036  123013  123014  117029  117006  121012  121049  103013  109015  121019  109057  121010  117034  103008  109038  109040  109034  117020  109029  111003  121015  109064  109009  117018  117030  109058  121016  109050  109076  117026  123022  109007  103001  111000  109071  109072  109075  121020  109090  109041  109039  109060  121047  123023  123024  117024  109088  121027  121069  109032  121009  121056  121057  109021  121034  121008  109048  109020  109036  109043  121058  109047  109031  109027  109028  109010  121071  109069  117014  123010  117009  121023  123015  123016  121041  109044  121037  121046  121072",
      "center_classification_date": "20170322",
      "distribution_pattern": "Distributed throughout the United States.",
      "state": "PA",
      "product_description": "ARTIS Q, Interventional Fluroscopic x-ray system",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1534-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76713",
      "termination_date": "20171024",
      "more_code_info": "",
      "recall_initiation_date": "20170222",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}