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FDAJanuary 13, 2015device

GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system

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

The hazard

It was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tome|x L240 installed had lost adhesion and fall out of position, which could lead to gaps in shielding.

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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