Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Combo Screw Driver (Product Code 288211) tip has...

Date: May 12, 2017
Company: DePuy Mitek, Inc., a Johnson & Johnson Co.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact DePuy Mitek, Inc., a Johnson & Johnson Co. directly.

Affected Products

DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

Quantity: 184 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 8 states: AZ, CA, CO, GA, MA, MI, OH, WA

Affected (8 states)Not affected

About DePuy Mitek, Inc., a Johnson & Johnson Co.

DePuy Mitek, Inc., a Johnson & Johnson Co. has 51 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report