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FDAApril 15, 2016device

GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.

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

The hazard

Potential non-recoverable loss of image acquisition. The affected Discovery systems may experience multiple X-Ray abort errors before or during a real-time fluoroscopic Interventional procedure.

What to do

FDA enforcement status: Terminated

Brands named

ge medical systems

UPCs

082416060019082416200019

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. Indicated for use in generating fluoroscopic and rotational images of human anatomy. — Recall Details · AllClear