{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98772",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355-1418",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "U.S. and O.U.S.",
      "recall_number": "Z-1814-2026",
      "product_description": "ARTIS Pheno VE30A and VE40A, Model 10849000",
      "product_quantity": "73",
      "reason_for_recall": "During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.",
      "recall_initiation_date": "20260312",
      "center_classification_date": "20260416",
      "report_date": "20260422",
      "code_info": "UDI 04056869046877"
    }
  ]
}