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GE Inspection Technologies, LP recalls GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Recalled April 13, 2016 · FDA recall Z-1231-2016 · GE Inspection Technologies
Hazard
GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i) · FDA Class II
Units
55 US Distribution
Sold at
US Distribution to the states of : TX, MD, MI, CA, TN, NH, NY, AL, NC, ID, MA, AZ, IN, FL, PA, NJ, WI, VA, MN, MD CO, GA, SC, OH and DC.
Description
GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)
Product
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Manufacturer(s)
GE Inspection Technologies, LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →