{
  "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": "Ongoing",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91383",
      "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": "Worldwide distribution",
      "recall_number": "Z-1001-2023",
      "product_description": "AXIOM Luminos Agile",
      "product_quantity": "271 units",
      "reason_for_recall": "There is potential for the footrest to detach from the patient table during use.",
      "recall_initiation_date": "20221209",
      "center_classification_date": "20230119",
      "report_date": "20230125",
      "code_info": "All serial numbers for AXIOM Luminos Agile, Material #10502200 (no UDI)"
    }
  ]
}