FDAMarch 17, 2015device

Head Holder shipped with Ingenuity Core 128 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.

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

The hazard

A head holder released for use with other CT systems but not yet qualified for use on the Ingenuity Core 128, which was shipped with this system.

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems clevelandphilipsphilips medical

UPCs

453567111331

Recall history

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

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