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

Recall date

January 13, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1211-2015

FDA classification

Class II

Brand / firm

GE Inspection Technologies, LP

Sold / distributed

US Distribution to the states of OH and PA.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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