Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert Recalled by Smith & Nephew, Inc. Due to The affected products were inadvertently packaged with the...
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 Smith & Nephew, Inc. directly.
Affected Products
smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 1-2 Size, 9 MM, REF 71453101designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact.
Quantity: 47 units
Why Was This Recalled?
The affected products were inadvertently packaged with the inner packaging pouch being sealed together with the outer pouch.
Where Was This Sold?
US, Canada, Great Britain, Australia, Italy, Germany, Malaysia, Singapore
About Smith & Nephew, Inc.
Smith & Nephew, Inc. has 220 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report