FDADecember 22, 2017device

LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended to provide to the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries.

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

The hazard

Reports of product loosening or coming unscrewed from the handle.

What to do

FDA enforcement status: Terminated

Brands named

depuy mitek inc a johnson johnsondepuydepuy mitek

Recall history

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

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