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FDAOctober 2, 2024device

smith&nephew GENESIS II NONPOROUS POSTERIOR STABILIZED FEMORAL COMPONENT, SIZE 5 LEFT, REF 71421015; Uncoated knee femur prosthesis, metallic

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 5N RIGHT implant instead of a GENESIS II POSTERIOR STABILIZED FEMORAL SIZE 5 LEFT as described on the product label.

What to do

FDA enforcement status: Ongoing

Brands named

smith nephewsmithsmith nephew

UPCs

03596010469212

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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