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FDADecember 31, 2018device

cone-beam CT system

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

The hazard

ORTHOPANTOMOGRAPH OP 3D device has a defect in the device firmware versions 2.1.0 and 2.1.1

What to do

FDA enforcement status: Ongoing

Brands named

kavo dental technologieskavokavo dental

Recall history

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

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