{
  "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": "2026-04-08",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "DAP chamber may be missing an insulating foil",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Material # 10308191  Serial # 13161",
      "center_classification_date": "20190709",
      "distribution_pattern": "IL, NE",
      "state": "PA",
      "product_description": "Cios Alpha VA20/ VA30 mobile X-Ray systems",
      "report_date": "20190717",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1953-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83255",
      "termination_date": "20200417",
      "more_code_info": "",
      "recall_initiation_date": "20190620",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}