{
  "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": "2026-04-08",
    "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": "81545",
      "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 Distribution to states of:  AR, CA, KS, KY, MD, MN, NM, OK, PA, RI, TX, and UT.",
      "recall_number": "Z-0558-2019",
      "product_description": "Artis Zee and Zeego, model no. 10272462    AXIOM Artis zee/Zeego is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.",
      "product_quantity": "64 (16 in US)",
      "reason_for_recall": "This recall has been initiated due to a possible leakage of a hose in the cooling unit of the X-ray tube.  The Artis zee system may lose coolant due to a possible leakage in a hose of the cooling unit in the X-ray tube. This will cause the X-ray tube not to be sufficiently cooled down. As a result, the system will display a message  Tube hot, have a break . The X-ray will be blocked several minutes later and to prevent any damage to the machine the following message will be displayed  NO XRAY, TUBE TOO HOT .  This issue is very sporadic and may occur during an ongoing clinical procedure.  Use of this product may have a potential impact on planned procedures as they may be delayed as well as in emergent cases, as clinical treatment may need to be terminated and transferred to a functioning system.",
      "recall_initiation_date": "20181026",
      "center_classification_date": "20181205",
      "termination_date": "20200512",
      "report_date": "20181212",
      "code_info": "Serial nos: 910045-09  911354-02  910045-19  908883-23  910045-15  910045-14  910045-25  908883-04  911354-25  908883-18  908883-11  910045-21  911354-26  908883-06  908883-02  911354-27"
    }
  ]
}