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FDADecember 10, 2014device

GE Healthcare, Discovery IGS 730 & Discovery IGS 740. Discovery IGS 730 : The angiographic X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular & non vascular diagnostic and interventional procedures. Discovery IGS 740:...

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

The hazard

Potential unintentional system motion or rotation due to a positioning user interface issue with Discovery IGS 730 and 740 products.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

UPCs

8241612004382416040061

Recall history

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

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GE Healthcare, Discovery IGS 730 & Discovery IGS 740. Discovery IGS 730 : The angiographic X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular & non vascular diagnostic and interventional procedures. Discovery IGS 740:... — Recall Details · AllClear