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GE Inspection Technologies, LP recalls GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily f
Recalled August 3, 2016 · FDA recall Z-2236-2016 · GE Inspection Technologies
Hazard
Radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system. The identified cause was insufficient attachment of shielding in the door. Jostling during delivery was identified as the probable cause of this failure to comply with the performance standard. · FDA Class II
Units
4
Sold at
US Distribution to the states of : FL, TN, and TX.
Description
Radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system. The identified cause was insufficient attachment of shielding in the door. Jostling during delivery was identified as the probable cause of this failure to comply with the performance standard.
Product
GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis.
Manufacturer(s)
GE Inspection Technologies, LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →