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FDAMarch 2, 2016device

GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis.

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Terminated

Brands named

ge inspection technologies lp

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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