{
  "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": "2026-03-18",
    "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": "91182",
      "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": "US Nationwide distribution in the states of CA, IA, LA, NE, NV, OH, SC.",
      "recall_number": "Z-0472-2023",
      "product_description": "ARTISTE, ONCOR and  PRIMUS with syngo RT Therapist with software version  4.3.1 MR3.    Material Number: 8162815  Intended Use:  Family of linear accelerator systems is to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer.",
      "product_quantity": "8 units US",
      "reason_for_recall": "When selecting the site fraction group for treatment, the User may select the wrong site for treatment, and potentially deliver the dose to wrong isocenter",
      "recall_initiation_date": "20221109",
      "center_classification_date": "20221209",
      "report_date": "20221221",
      "code_info": "UDI: N/A S/N: 10736, 10737, 10822, 10850, 10886,10843, 10865,10025 Software version 4.3.1 MR3"
    }
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}