Home / Recalls / Medical Devices
GE Inspection Technologies, LP recalls GE Cabinet X-ray systems
Recalled December 24, 2014 · FDA recall Z-0426-2015 · GE Inspection Technologies
Hazard
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards. · FDA Class II
Units
11
Sold at
US Distribution to the states of MI, PA, NH, CA, OR, WA, NC, IN and SC.
Description
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
Product
GE Cabinet X-ray systems
Manufacturer(s)
GE Inspection Technologies, LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →