Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Device is missing the pin in the graft...
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
COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
Quantity: US: 131 units; OUS: 312 units
Why Was This Recalled?
Device is missing the pin in the graft loader component.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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