{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "The Ysio system may process incorrect internal values for the position of its ceiling tube stand. If in this situation the user activates longitudinal or transversal stand movement (by using the buttons at the tube head or the remote console), the system\u0019s controls may (depending on the values being processed) initiate a \u001ccorrection\u001d of the tube stand position, resulting in an unexpected movement.",
      "address_2": "",
      "product_quantity": "81 US/ 308 worldwide",
      "code_info": "Serial Nos. 20113  20034  21100  21086  21113  21088  21103  21221  21223  21224  21085  20045  20093  20110  21066  21031  21139  21006  20155  21112  21122  21185  20088  20089  20106  20107  21052  21089  21213  20167  21098  21174  21057  21101  21116  21117  21118  21120  21091  21092  21037  21076  21077  21200  21203  21209  20149  21163  21172  21171  21173  20094  21115  20047  21194  20193  21211  21212  21186  21188  21094  21039  21040  21108  20035  20185  21061  21065  21205  21095  21148  21189  21140  21175  21023  21001  21127  21123  21013  20159  21160",
      "center_classification_date": "20200316",
      "distribution_pattern": "US Nationwide distribution in the states of AR, CA, DC, FL, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NV,   NY, OH, OR, PA, SC, TX, UT, VA and WI.",
      "state": "PA",
      "product_description": "Ysio, model no. 10281013    Product Usage: The product is a stationary X-Ray system.",
      "report_date": "20200325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1501-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85029",
      "termination_date": "20200831",
      "more_code_info": "",
      "recall_initiation_date": "20200210",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}