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DePuy Mitek, Inc., a Johnson & Johnson Co. recalls LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intende
Recalled May 16, 2018 · FDA recall Z-1749-2018 · DePuy Mitek, Inc., a Johnson & Johnson
Hazard
Reports of product loosening or coming unscrewed from the handle. · FDA Class II
Units
84
Sold at
US Nationwide Distribution in the states of OH, WA, CO
Description
Reports of product loosening or coming unscrewed from the handle.
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.
Manufacturer(s)
DePuy Mitek, Inc., a Johnson & Johnson Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →