DePuy Mitek, Inc., a Johnson & Johnson Co.: Medical Device Recall in 2018 - (Recall #: Z-1749-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: December 22, 2017

Date Posted: May 16, 2018

Recall Number: Z-1749-2018

Event ID: 79518

Reason for Recall:

Reports of product loosening or coming unscrewed from the handle.

Status: Terminated

Product Quantity: 84

Code Information:

16D01,16D02, 16K01, 17A01, 17B01, 17B02

Distribution Pattern:

US Nationwide Distribution in the states of OH, WA, CO

Voluntary or Mandated:

Voluntary: Firm initiated