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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

GE Healthcare, LLC recalls System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to suppo | RecallWatchUSA