Recall Z-1288-2021 — Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
U.S. FDA — Device Enforcement · United States · 2021-02-26 · Class II
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Reported risk: Siemens has become aware of a potential issue in which the imaging system UPS sporadically forces a shutdown of the imaging system PC without a true power supply problem.
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