{
  "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": "2026-07-08",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94777",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2184-2024",
      "product_description": "AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining  emergency and accident patients as well as for use in outpatient departments.  Material Number:  MD39543",
      "product_quantity": "2 units",
      "reason_for_recall": "Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire",
      "recall_initiation_date": "20240531",
      "center_classification_date": "20240625",
      "report_date": "20240703",
      "code_info": "UDI-DI: N/A  Serial Numbers: 1040 1020",
      "more_code_info": ""
    }
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}