Discovery NM/CT 670 ES, model 5376204-70-57
Check against the official notice below — it lists the full affected range.
GE Healthcare has recalled 2 units of the Discovery NM/CT 670 ES model 5376204-70-57 due to potential wiring defects in safety shutoff components. During installation, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) may not have been wired correctly, which could prevent these controls from shutting off all power to the system as intended, creating a potential electric hazard.
The affected units were distributed in California, the District of Columbia, Ohio, Utah, Wisconsin, and Canada. The recalled devices have GTIN 00840682123877 and include serial numbers ESDX35013 and ESDW35010. The source document does not specify what remedy is available to 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: 2 units Lot/code info: GTIN 00840682123877 Serial Numbers: ESDX35013, ESDW35010
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.