FDAMay 24, 2018device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Completed

Brands named

ge healthcare

UPCs

0084068212439353762047056

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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