Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Combo Screw Driver (Product Code 288211) tip has...
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 Drill Product Code: 288201 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
About DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek, Inc., a Johnson & Johnson Co. has 51 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report