DePuy Mitek, Inc., a Johnson & Johnson Co.: Medical Device Recall in 2017 - (Recall #: Z-2618-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

Product Classification:

Class II

Date Initiated: May 12, 2017

Date Posted: June 28, 2017

Recall Number: Z-2618-2017

Event ID: 77252

Reason for Recall:

Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw

Status: Terminated

Product Quantity: 153 units

Code Information:

GTN: (01)10886705026814 Lot codes: 16D01, 16D02, 16E01, 16J01, 16R01, 17A01, 17A02, 17C03

Distribution Pattern:

US: AZ, CA, CO, GA, MA, MI, OH, WA Foreign: Austria, Australia, Belgium, France, Germany, Spain, Switzerland, Netherlands, Poland, UK

Voluntary or Mandated:

Voluntary: Firm initiated