{
  "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   10762473 with serial numbers: 4014  4056  4015  4063  4022  4036  4043  4024  4059  4020  4032  4053  4061  4060  4051  4025  4037  4054  4042  4033  4055  4052  4047  4049  4038  4062",
      "center_classification_date": "20150523",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "PA",
      "product_description": "SIEMENS Uroskop Omnia Max ; a solid state detector fluoroscopic X-Ray system, primarily for urological applications (functional x-ray diagnostic, endourology and minimal invasive urology/surgery). The system,, which includes a radiologic/urologic treatment table, may be used for urological, gastroenterological and gynecological treatment, planning and diagnostic procedures including but not limited to: Querying and retrieving patient history information and/or previous diagnosis and images from other modalities, including X-ray examinations of the urogenital area, Ultrasound examinations, Endourological interventions, Percutaneous interventions, Laparoscopy, Application of fistula, Simple procedures, Extracorporeal shock wave lithotripsy, Uroflow/urodynamics, Pediatric radiological and therapeutic applications.",
      "report_date": "20150603",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1670-2015",
      "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"
    }
  ]
}