GE Healthcare, LLC: 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.

Agency Publication Date: December 13, 2018

Affected Products

Product: Discovery NM/CT 670 DR, model 5376204-70-56 intended for use in detecting, localizing, diagnosing of diseases and organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer.

GTIN 00840682124393 Serial Numbers: DDRW34032, DDRX34038, DDRX34041, DDRX34045

Product: Discovery NM/CT 670 ES, model 5376204-70-57

GTIN 00840682123877 Serial Numbers: ESDX35013, ESDW35010

Product: Discovery NM/CT 670 Pro, model 5376204-70-54

GTIN 00840682121194 Serial Number ESDX35015

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 81680

Status: Resolved

Manufacturer: GE Healthcare, LLC

Manufactured In: United States

Units Affected: 3 products (4 units; 2 units; 1 unit)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

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