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Smith & Nephew, Inc. recalls smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 1-2 Size, 9 MM, REF 71453101designed for use in patients in
Recalled May 30, 2018 · FDA recall Z-1907-2018 · Smith & Nephew
Hazard
The affected products were inadvertently packaged with the inner packaging pouch being sealed together with the outer pouch. · FDA Class II
Units
47 units
Sold at
US, Canada, Great Britain, Australia, Italy, Germany, Malaysia, Singapore
Description
The affected products were inadvertently packaged with the inner packaging pouch being sealed together with the outer pouch.
Product
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.
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →