FDAFebruary 23, 2017device

Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient an...

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

The hazard

Philips identified a 4D CT pulmonary phase issue on Brilliance BigBore Oncology/Radiology CT with 4.2.0 software version through customer complaints. When the user performs a retrospective respiratory gated 4D CT scan with the Bellows pulmonary gating device, the CT images might be reconstructed at a single phase, while the annotations on the images incorrectly indicate that the reconstruction is from the requested specific phases (0% to 90%).

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems clevelandphilipsphilips medical

UPCs

00884838059450

Recall history

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

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Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient an... — Recall Details · AllClear