{
  "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": "2026-04-15",
    "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": "86250",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Natonwide distribution.",
      "recall_number": "Z-0108-2021",
      "product_description": "Artis zee or Artis Q systems (listed below) - Product Usage: for single and biplane diagnostic imaging and interventional procedures.    System Name/Material Number:  Artis Q BIPLANE\t10848282  ARTIS Q CEILING\t10848281  Artis Q floor\t10848280  ARTIS Q ZEEGO\t10848283  ARTIS Q.ZEN BIPLANE\t10848355  ARTIS Q.zen ceiling\t10848354  Artis Q.zen floor\t10848353  Artis zee Biplane\t10094141  Artis zee ceiling\t10094137  Artis zee floor\t10094135  Artis zee floor\t10094135  Artis zee multi-purpose\t10094139  Artis zeego\t10280959",
      "product_quantity": "124 U.S",
      "reason_for_recall": "Potential exists for the collision supervision not to work properly following loss of the individual room configuration data settings causing danger of collision with fix mounted room equipment, walls or floor may occur. This might cause components of the system to fall or tilt which could result in crushing of patients, operators or staff, collision of system parts with patients, as well as result in delay or interruption of the clinical procedure",
      "recall_initiation_date": "20200803",
      "center_classification_date": "20201015",
      "termination_date": "20210203",
      "report_date": "20201021",
      "code_info": "Software VD11C Patch distributed earlier via Update Instructions AX030/19/S or AX051/19/P.  Serial Numbers:  103222  103285  103286  105016  109016  109021  109069  109105  109107  109158  109163  109189  109221  109300  109331  109367  109371  109393  109416  109451  109460  109504  109505  109520  111005  111104  111106  111117  111120  111123  111125  117014  117030  117117  117123  117129  117134  117303  117309  117310  117314  117325  117329  117330  121008  121058  121062  121071  121375  121377  121378  121383  121405  121417  121442  123010  123014  123023  123049  123208  123209  123233  124286  125201  125233  137245  137421  137438  137479  137729  138102  138104  138147  138156  138201  146323  147516  147612  147652  147670  147676  147724  147745  147880  147905  147923  147925  147926  147928  147944  148207  148282  148349  154532  154612  154633  154663  154739  155151  157704  158032  158458  158474  158552  160431  160449  160494  160509  160845  160850  160861  160885  160913  160942  160953  160959  160978  160999  161004  161008  161021  161050  161224  161226"
    }
  ]
}