{
  "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 systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.",
      "address_2": "",
      "product_quantity": "459 (116 US)",
      "code_info": "Serial Number 105121  105122  105123  105124  105125  111129  111130  111127  111106  111128  123245  123246  123240  123239  123244",
      "center_classification_date": "20190515",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of  AL,AR, AZ, CA, FL, ID, IL, IN, KS, LA, MA, MD, MI, MN,   MO, NC, ND, NE, NV, NY, OH, OK, OR, PA, RI, SC, SD, TX, UT,  VA , WA WI and WV. and Foreign countries.",
      "state": "PA",
      "product_description": "Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen 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 AXIOM Artis zee and Q/ Q.zen family include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. AXIOM Artis zee and Q/ Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis.",
      "report_date": "20190522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1342-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82730",
      "termination_date": "20200423",
      "more_code_info": "",
      "recall_initiation_date": "20190409",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}