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Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interv
Recalled March 31, 2021 · FDA recall Z-1288-2021 · Siemens Medical Solutions USA
Hazard
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. · FDA Class II
Units
29 systems
Sold at
US Nationwide distribution in the states of MI, KY, TX.
Description
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.
Product
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.
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →