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GE Inspection Technologies, LP recalls GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Recalled August 9, 2017 · FDA recall Z-2777-2017 · GE Inspection Technologies
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. · FDA Class II
Units
13 units distributed in the US
Sold at
US Distribution to the states of : AL, SC, OH, MI, PA, and Internationally to Germany and Singapore
Description
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.
Product
GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Manufacturer(s)
GE Inspection Technologies, LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →