FDASeptember 15, 2014device

GE OEC Brivo 715 Prime Mobile C-Arm X-Ray Product Used for general surgical applications and musculoskeletal procedures to visualize.

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

The hazard

mA Accuracy may exceed the design and labeling specification of+ 10%. Per 1020.32(f): Deviation of x-ray tube potential and current from the indicated values shall not exceed the maximum deviation as stated by the manufacturer in accordance with 1020.30(h)(3).

What to do

FDA enforcement status: Terminated

Brands named

ge oec medical systems

Recall history

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

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