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Recall Observatory FDA recall evidence

Device product

Siemens Uroskop Omnia Max system The Uroskop Omnia is 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; "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

Z-0004-2015

September 02, 2014

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 69258
Status
Terminated
Classification
Class II
Quantity
2
Official record key
device-enforcement:Z-0004-2015

Official wording

Reason: Two malfunctions posing potential risk to patients were identified with Siemens Ysio Max, AXIOM Luminos dRF Max, Uroskop Omnia Max, and Luminos Agile Max systems with a specific set of serial numbers that will cause lost images due to an automatic Radiology Information System (RIS) worklist update, thus causing examinations to be repeated. Image label may also be displayed incorrectly after images

Code information: Siemens Uroskop Omnia Max system, material #s: 10762473, serial numbers: 4014 4015

Distribution pattern: Nationwide Distribution - US including UT, MO, CO, MA, MN, MS, OH, SC, MI, and NY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Two malfunctions posing potential risk to patients were identified with Siemens Ysio Max, AXIOM Luminos dRF Max, Uroskop Omnia Max, and Luminos Agile Max systems with a specific set of serial numbers that will cause lost images due to an automatic Radiology Information System (RIS) worklist update, thus causing examinations to be repeated. Image label may also be displayed incorrectly after images