{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "51 Valley Stream Pkwy",
      "reason_for_recall": "A cable inside the C-arm systems may have been routed in an inappropriate manner.  Improper routing of the cable may result in increased wear over time. Without additional measures, the potential exists for a cable inside the C-arm to break which could result in restricted functionality or system failure and an ongoing procedure could be terminated.  Additionally, a subgroup of affected C-arm systems will receive a replacement of the cable harness.",
      "address_2": "",
      "product_quantity": "164",
      "code_info": "model number 10280959, with serial numbers 1000-1599",
      "center_classification_date": "20141107",
      "distribution_pattern": "Nationwide Distribution including Puerto Rico.",
      "state": "PA",
      "product_description": "Artis zeego systems, model number 10280959, with serial numbers 1000-1599 : Artis zeego is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.  Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.",
      "report_date": "20141119",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0183-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69480",
      "termination_date": "20170508",
      "more_code_info": "",
      "recall_initiation_date": "20140923",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}