FDAAugust 5, 2015device

Owandy Radiology I -MAX Touch 3D X-ray

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

The hazard

It has been discovered that due to lack of information accompanying documents the product fails to comply with 21CfR 1020.33(c),1020.33(d),1020.33(g),and 1020.330).

What to do

FDA enforcement status: Terminated

Brands named

villa radiology systemsvillavilla radiology

Recall history

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

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