{
  "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": "83203",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2023-2019",
      "product_description": "AXIOM Artis dMP, Model Number 7555365",
      "product_quantity": "32",
      "reason_for_recall": "A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.",
      "recall_initiation_date": "20190612",
      "center_classification_date": "20190722",
      "termination_date": "20200918",
      "report_date": "20190731",
      "code_info": "Serial Numbers: 57204  57089  57077  57024  57144  57189  57208  57035  57188  57073  57072  57016  57009  57050  57207  57111  57171  57113  57193  57008  57198  57155  57124  57004  57105  57098  57116  57045  57156  58701  57183  57187"
    }
  ]
}