FDADecember 3, 2019device

Exactech equinoxe PLATFORM FRACTURE, HUMERAL STEM, CEMENTED, Right, 10.5mm, REF 304-22-11 - Product Usage: The Equinoxe Shoulder System is indicated for use and in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint work total or hemi- arthroplasty is d...

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

The hazard

Labels with incorrect translations were identified by Exactech is a distributor in the Netherlands. The translations on the outer labels include the word " long" in all languages other than the original English version. The implants are standard length fracture stems.

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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