Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily Recalled by Hans Pausch Rontgengeratebau Gmbh Due to During patient interventions with the urology table the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hans Pausch Rontgengeratebau Gmbh directly.
Affected Products
Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily for urological applications (functional X-ray diagnostics, endourology and minimal invasive urology / surgery). The system, which includes a radiologic / urologic treatment table, maybe used for urological treatment, planning and diagnostic procedures, including but not limited to.
Quantity: 10 systems
Why Was This Recalled?
During patient interventions with the urology table the radiation is activated with a footswitch connected to the table. This footswitch is actively involved in the safety circuit of the urological table. Only if footswitch + exposure + first primary barrier are closed the signal will be transmitted to the generator for activating X-ray. During intended use only with this footswitch X-ray should be activated.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hans Pausch Rontgengeratebau Gmbh
Hans Pausch Rontgengeratebau Gmbh has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report