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Eos Imaging Inc recalls EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.
Recalled October 10, 2012 · FDA recall Z-2072-2012 · Eos Imaging
Hazard
It was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode. · FDA Class II
Units
12 EOS Systems installed in the US
Sold at
Nationwide distribution
Description
It was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode.
Product
EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.
Manufacturer(s)
Eos Imaging Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →