Discovery NM/CT 670 Pro, model 5376204-70-54
Check against the official notice below — it lists the full affected range.
GE Healthcare, LLC is recalling the Discovery NM/CT 670 Pro model 5376204-70-54 because the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) may not have been wired correctly during installation. This wiring problem could prevent these controls from shutting off all power to the entire system as intended, creating a potential electric hazard. One unit with serial number ESDX35015 (GTIN 00840682121194) was distributed in California, the District of Columbia, Ohio, Utah, Wisconsin, and Canada.
The recall record does not specify a remedy or corrective action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Reason for recall: 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. Distribution: CA, DC, OH, UT, WI, Canada Quantity: 1 unit Lot/code info: GTIN 00840682121194 Serial Number ESDX35015
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.