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FDADecember 16, 2015device

GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.

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

The hazard

GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)

What to do

FDA enforcement status: Terminated

Brands named

ge inspection technologies lp

Recall history

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

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