medical Class II Updated 2018-05-16

DePuy Mitek, Inc., a Johnson & Johnson Co. recalls LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage:

Recalled Product

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.


Hazard / Issue

Reports of product loosening or coming unscrewed from the handle.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 16D01,16D02, 16K01, 17A01, 17B01, 17B02
View official government recall

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