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GE Healthcare, LLC recalls Discovery NM/CT 670 Pro, model 5376204-70-54
Recalled December 19, 2018 · FDA recall Z-0608-2019 · GE Healthcare
Hazard
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard. · FDA Class II
Units
1 unit
Sold at
CA, DC, OH, UT, WI, Canada
Description
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.
Product
Discovery NM/CT 670 Pro, model 5376204-70-54
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →