{
  "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": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83082",
      "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",
      "recall_number": "Z-1903-2019",
      "product_description": "Siemens Artis Q.zen ceiling-Interventional Fluoroscopic X-Ray System  Model Number: 10848354",
      "product_quantity": "15",
      "reason_for_recall": "Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off,  can result in severe injuries to patients and operating personnel",
      "recall_initiation_date": "20190606",
      "center_classification_date": "20190628",
      "termination_date": "20210209",
      "report_date": "20190710",
      "code_info": "Serial Numbers:  111005  111000  111002  111125  111123  111109  111128  111124  111122  111104  111106  111121  111127  111137  111135"
    }
  ]
}