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FDAMarch 29, 2018device

Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems

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

The hazard

The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of imaging mode before or during fluoroscopic use.

What to do

FDA enforcement status: Terminated

Brands named

ge medical systems scs

UPCs

082416160071082416040075082416110059082416160068082416120077082416120092082416030051082416160075082416100140082416090100082416100152082416140030

Recall history

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

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