FDANovember 4, 2015device

Copper NiTi Preformed Archwires; Copper NiTi 40 BAF .016X.022 LO Pk10, Part No. 211-0952. Intended to provide tooth movement.

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

The hazard

Ormco Corporation is recalling Copper NiTi Preformed Archwires because the product transformation temperature as listed on the labeling is incorrect.

What to do

FDA enforcement status: Terminated

Brands named

ormco sybronendoormcoormco sybronendo

Recall history

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

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