Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
smith&nephew LEIGON OXINIUM CONSTRAINED NONPOROUS FEMORAL COMPONENT Recalled by Smith & Nephew Inc Due to Complaint received indicating that a package contained a...
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 LEIGON OXINIUM CONSTRAINED NONPOROUS FEMORAL COMPONENT, SIZE 3 LEFT, REF 71421163; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
Quantity: 3 units
Why Was This Recalled?
Complaint received indicating that a package contained a LGN OX CONSTRAINED FEM 3 LT implant instead of a LGN OX CONSTRAINED FEM 4 LT as described on the product label.
Where Was This Sold?
US Distribution to state of Texas and OUS (foreign) to countries of: Spain, France and United Kingdom,.
About Smith & Nephew Inc
Smith & Nephew Inc has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report