{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65491",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "address_2": "N/A",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution including the states of  CA, IN, NJ and OK.",
      "recall_number": "Z-1848-2013",
      "product_description": "Siemens Luminos dRF Fluoroscopic X-Ray system    Fluoroscopic X-Ray system",
      "product_quantity": "4",
      "reason_for_recall": "Siemens became aware of an unintended behavior when using the Luminos dRF with software version VD10A.  The possibility exists that a software error may occur causing the table to tilt into an upright position and may collide with the floor.  Four consignees were notified of this recall by Update Instruction XP067/12/S -- all four units have been corrected.",
      "recall_initiation_date": "20130507",
      "center_classification_date": "20130801",
      "termination_date": "20131224",
      "report_date": "20130807",
      "code_info": "Model number 10094200, serial numbers 4024, 4077, 4043 and 4051",
      "more_code_info": ""
    }
  ]
}