{
  "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": "51 Valley Stream Pkwy",
      "reason_for_recall": "The firm became aware of a potential issue with Axiom Artis systems installed by a third party installer that may involve  incorrect channel nuts being used.",
      "address_2": "",
      "product_quantity": "178",
      "code_info": "Multiple Model numbers: 10281163, 10281013, 10280959, 10272410, 10094200, 10094142, 10094141, 10094139, 10094137, 10094135, 10093961, 10093902, 8890415, 8890407, 8627718, 8395431, 8395415, 8395399, 8395381, 7728392, 7555373, 755365, 7555357, 7412807, 7151066, 7008605, 5904441, 5904433, 5895003, 475525, 475517, 475509.",
      "center_classification_date": "20130828",
      "distribution_pattern": "US Distribution including the states of  PA, NJ, DC, VA, MD and DE.",
      "state": "PA",
      "product_description": "Axiom Artis systems. C-arm angiographic x-ray system    x-ray, angiographic system.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-2108-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65793",
      "termination_date": "20141106",
      "more_code_info": "",
      "recall_initiation_date": "20130426",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}