medical Class II Updated 2024-11-06

Smith & Nephew Inc recalls smith&nephew LEIGON OXINIUM CONSTRAINED NONPOROUS FEMORAL CO

Recalled Product

smith&nephew LEIGON OXINIUM CONSTRAINED NONPOROUS FEMORAL COMPONENT, SIZE 4 LEFT, REF 71421164; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER


Hazard / Issue

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.

Issued by

FDA

Distribution: US Distribution to state of Texas and OUS (foreign) to countries of: Spain, France and United Kingdom,.
Lot/Code Info: UDI/DI 03596010543837, Batch Number 23LM03388
View official government recall

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