DePuy Mitek, Inc., a Johnson & Johnson Co.: Medical Device Recalls in 2018

According to to data from the FDA, there were 3 medical device recalls made by DePuy Mitek, Inc., a Johnson & Johnson Co. in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Gravity Tube Set is intended to deliver irrigation fluid from irrigation containers to the operative site during arthroscopic procedures.
• 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.
• Mitek Screw and Washer Depth Gauge, Product Code 219024