FDASeptember 25, 2020device

Equinoxe Platform Fracture Stem, 6.5mm, Right - Product Usage: The Equinoxe Platform Fracture Stem is indicated for cemented use only.

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

The hazard

The device may be incorrectly laser marked as a right stem, when it should have been laser marked as a left stem.

What to do

FDA enforcement status: Terminated

Brands named

exactech

UPCs

49712924971303

Recall history

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

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