{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "51 Valley Stream Pkwy",
      "reason_for_recall": "During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.",
      "address_2": "",
      "product_quantity": "284",
      "code_info": "Artis zee Ceiling systems serial numbers from 146352 to 147617",
      "center_classification_date": "20140224",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "PA",
      "product_description": "Siemens Artis zee Ceiling Systems.    Angiographic x-ray system.",
      "report_date": "20140305",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1080-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67175",
      "termination_date": "20150309",
      "more_code_info": "",
      "recall_initiation_date": "20131216",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}