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GE Inspection Technologies, LP recalls GE Optional Laser Centering Device X-ray generator.
Recalled August 19, 2015 · FDA recall Z-2320-2015 · GE Inspection Technologies
Hazard
GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device. · FDA Class II
Units
25
Sold at
US Distribution to the states of : NY, CA, WA, PA, MD, AL, FL and LA.
Description
GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.
Product
GE Optional Laser Centering Device X-ray generator.
Manufacturer(s)
GE Inspection Technologies, LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →