{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72138",
      "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": "Nationwide Distribution.",
      "recall_number": "Z-0118-2016",
      "product_description": "CIOS ALPHA; image intensified fluoroscopic x-ray system",
      "product_quantity": "44",
      "reason_for_recall": "patient procedure interruption due to a potential system failure",
      "recall_initiation_date": "20150817",
      "center_classification_date": "20151023",
      "termination_date": "20161205",
      "report_date": "20151104",
      "code_info": "model #10308191 with serial numbers: Serial  11032  10073  11132  11044  11005  10115  11056  10057  10076  10019  10035  11074  11075  11077  11083  11124  10078  11119  11103  11105  11013  10021  10037  10063  11106  10082  11098  11094  10089  11080  11009  11018  11082  10058  10098  11120  11134  11015  11016  11038  10116  11035  11107  11064"
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}