FDAJune 28, 2017device

GE Inspection Technologies Blade|line Industrial Cabinet X-ray system

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

The hazard

GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the cabinet x-ray performance standards emission limit of 0.5 milliRoentgen in one hour (21 CFR ¿ 1020.40(c)(1)(i)) underneath the bottom center of the system. The crawl space affected by the excess emission is approximately 22 inches high, normally covered by decorative panels, and is not intended to be accessed.

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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GE Inspection Technologies Blade|line Industrial Cabinet X-ray system — Recall Details · AllClear