Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical Technology, Inc. Due to Two lots of Ortholoc 3Di Fusion plates contain...
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 Wright Medical Technology, Inc. directly.
Affected Products
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
Quantity: 41 units
Why Was This Recalled?
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Wright Medical Technology, Inc.
Wright Medical Technology, Inc. has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report