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GE Healthcare, LLC recalls System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to suppo
Recalled October 28, 2020 · FDA recall Z-0130-2021 · GE Healthcare
Hazard
Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet. · FDA Class II
Units
30 devices Total
Sold at
Worldwide distribution - US Nationwide distribution including in the states of FL, KY, NC, NJ, NM, NY, TX, UT and WA. The countries of Canada, Hungary, India, Korea, China, Russia, Taiwan, Puerto Rico and Ubekistan.
Description
Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Product
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →