{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "Potential hardware issue which may cause thermal effects and possible damage to system parts.",
      "address_2": "",
      "product_quantity": "605 units in total",
      "code_info": "Serial Numbers:  164033  164071  164034  164095  164057  164054  164055  164080  164072  164088  164048  164094  164068  164019  164013  164073  164025  164026  164027  164060  164083  164113  164021  164066  164075  164074  164084  164086  164098  164028  164053  164063  164064  164105  164024  164049  164018  164022  164061  164115  164100  164097  164011",
      "center_classification_date": "20180810",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PA",
      "product_description": "ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System    Product Usage:  Artis 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. Procedures that can be performed with the Artis family include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis can also support the acquisition of position triggered imaging for spatial data synthesis.",
      "report_date": "20180822",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-2748-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80586",
      "termination_date": "20200115",
      "more_code_info": "",
      "recall_initiation_date": "20180622",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}