FDAMay 25, 2017device

EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #: 321-45-38, Catalog #: 321-45-42 and Catalog #: 321-45-46

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

The hazard

Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-axis and that reaming off-axis may result in instrument breakage.

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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