{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "51 Valley Stream Pkwy",
      "reason_for_recall": "Study and all acquired images deleted when using systems with software version VE10E.  Acquisitions have to be repeated.  Connection with portable detectors (MAX wi-D, MAX mini) is sporadic in image recovery.  Pressing undo button on the RAD subtask card or previous series button on the Image subtask card during image readout. Sporadically, during an automatic or a manual RIS update.",
      "address_2": "",
      "product_quantity": "133 total",
      "code_info": "Model Number of device    10762472 with serial numbers: 61034  61052  61045  61013  61054  61056  61021  61050  61053  61032  61015  61046  61028  61040  61011  61029  61048  61060  61042  61035  61014  61025  61043  61036  61038  61022  61037  61049  61044  61062  61030  61018  61027  61061  61033  61039  61047  61031  61041  61055  61019  61057  61059  61017  61051",
      "center_classification_date": "20150523",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "PA",
      "product_description": "SIEMENS Luminos Agile Max; a universal imaging system for radiographic and fluoroscopic studies. Using either film cassettes or a digital mobile flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. Luminos Agile is applicable to emergency treatment on an outpatient basis, as well as for bedside examinations.",
      "report_date": "20150603",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1669-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71115",
      "termination_date": "20170320",
      "more_code_info": "",
      "recall_initiation_date": "20150413",
      "postal_code": "19355-1406",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}