FDAOctober 6, 2020device

Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium

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

The hazard

The product may be mislabeled.

What to do

FDA enforcement status: Terminated

Brands named

exactech

Recall history

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

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Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium — Recall Details · AllClear