{
  "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": "In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.",
      "address_2": "",
      "product_quantity": "3",
      "code_info": "Model Number: 10094142  Serial Number: 140422, 140423, 140430  Software Version: VC21C",
      "center_classification_date": "20191217",
      "distribution_pattern": "US: WA and TX  International: Denmark",
      "state": "PA",
      "product_description": "Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C",
      "report_date": "20191225",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0695-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84370",
      "termination_date": "20200512",
      "more_code_info": "",
      "recall_initiation_date": "20191114",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}